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BIOMET 3I, LLC

Last updated May 24, 2026

What BIOMET 3I, LLC makes

BIOMET 3I, LLC manufactures dental implants and related products, including screw endosteal implants, both permanent and temporary suprastructure components, dental drill bits (reusable and single-use), surgical screwdrivers, and bone taps.

The company's products are regulated as Class I and Class II medical devices and are listed in the FDA UDI registry. BIOMET 3I, LLC is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does BIOMET 3I, LLC manufacture?

BIOMET 3I, LLC manufactures dental implants and related products, including screw endosteal dental implants, both permanent and temporary dental implant suprastructure components, dental drill bits (reusable and single-use), surgical screwdrivers, bone taps, and dental regeneration membranes.

Where is BIOMET 3I, LLC based?

BIOMET 3I, LLC is based in the United States, as indicated by the country information provided in the device data.

Which regulatory registries list BIOMET 3I, LLC's devices?

BIOMET 3I, LLC's devices are listed in the FDA UDI registry, which is the only registry mentioned in the provided device data for this company.

How are BIOMET 3I, LLC's devices classified?

BIOMET 3I, LLC's devices are regulated as Class I and Class II medical devices, with Class II being the most common classification for their dental implant products and related components.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: biomet.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(800)342-5454
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 186127825

Catalogue (2523)

Page 27 of 51

Device	Model / Reference	Registries	Class	Status
Osseotite®	FNT515	FDA UDI	Class II	Active
3i T3® DCD®	BNPS4310	FDA UDI	Class II	Active
Certain®	IPPIA5	FDA UDI	Class I	Active
Certain® Bellatek® Encode®	IEHA664	FDA UDI	Class II	Active
Osseotite Nt®	NTDI3215	FDA UDI	Class I	Active
Navigator®	SGTT410L	FDA UDI	Class I	Active
3i T3®	BOES411	FDA UDI	Class II	Active
Certain® Iol®	IIOL55S	FDA UDI	Class II	Unknown
Ep®	WTH672	FDA UDI	Class II	Active
Certain® Bellatek®	IEDAT3	FDA UDI	Class II	Active
Preformance®	PFTC42	FDA UDI	Class II	Active
Osseotite Nt®	NTDI685	EUDAMEDFDA UDI	Class I	Active
Certain® Bellatek® Encode®	IEHA456	FDA UDI	Class II	Active
Nanotite™certain®prevail®	NIITP5415	FDA UDI	Class II	Active
Nanotite®	NNT3210	FDA UDI	Class II	Unknown
Bellatek®	CSHY06	FDA UDI	Class II	Active
Navigator®	MSGTT15L	EUDAMEDFDA UDI	Class I	Active
Bellatek®	CSD06	FDA UDI	Class II	Active
Immediate Molar	IMDR58	FDA UDI	Class I	Active
Ltx	LTX3213	FDA UDI	Class II	Unknown
3i T3®	BOET685	FDA UDI	Class II	Active
3i T3® DCD®	BNES518	FDA UDI	Class II	Active
Immediate Molar	IMDIR34	FDA UDI	Class I	Active
Immediate Molar	IMDR44TSXSP	FDA UDI	Class I	Active
Bellatek®	TSVZLDAT3	FDA UDI	Class II	Active
Act®	ACTPSD	EUDAMEDFDA UDI	Class I	Active
Osseotite®	OSS318	FDA UDI	Class II	Active
Osseotite® Certain®	XIFNT610	FDA UDI	Class II	Active
Ep®	TH253	FDA UDI	Class II	Unknown
Certain® Bellatek®	I3MAT6	FDA UDI	Class II	Active
TSX Implants	TSX47B13	FDA UDI	Class II	Active
Osseotite® 2	XFOS685	FDA UDI	Class II	Active
Ep®	WT2556	FDA UDI	Class II	Unknown
Certain® Bellatek® Encode®	IEHA356	FDA UDI	Class II	Active
Regeneross®	ROAPM10	FDA UDI	Class II	Active
Immediate Molar	IMDR86SP	FDA UDI	Class I	Active
Regeneross®	ROAP05	FDA UDI	Class II	Active
Ep®	WIP56	FDA UDI	Class I	Active
Osseoguard®	TR150RAKL-N-2	FDA UDI	Class II	Active
Certain® Gingihue®	IWPP664G	FDA UDI	Class II	Active
Certain® Prevail®	IIOS5415	FDA UDI	Class II	Unknown
Navigator®	SGD325D	FDA UDI	Class I	Active
Osseotite Xp®	OS4510	FDA UDI	Class II	Unknown
Nanotite®	NOSS685	FDA UDI	Class II	Unknown
Osseotite® Certain®	IOSS411	FDA UDI	Class II	Active
Certain®	ISWHA56	FDA UDI	Class II	Active
Osseotite® 2	XFOS610	FDA UDI	Class II	Active
Certain® Prevail®	IIOS3410	FDA UDI	Class II	Unknown
Osseoguard®	TR250PR-2	FDA UDI	Class II	Active
Ratchet Hex Driver with GemLock Retention 2.5mm (D) X 17mm (L)	GHX2.5	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (100)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Biomet 3i, LLC has 240 recall records initiated between 2006-12-11 and 2020-08-31, all with a status of terminated. The reasons for recall include mislabeling of packages, potential sterility issues, inadequate biocompatibility testing, seating problems, incorrect manufacturing of internal threads and hex features, drill malfunctions, reports of abutment fractures, and oversized copings.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Aug 31, 2020	Z-0077-2021	—	terminated	Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient
Aug 31, 2020	Z-0076-2021	—	terminated	Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient
Aug 31, 2020	Z-0078-2021	—	terminated	Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient
Aug 31, 2020	Z-0075-2021	—	terminated	Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient
Aug 31, 2020	Z-0074-2021	—	terminated	Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient
Aug 31, 2020	Z-0073-2021	—	terminated	Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient
Aug 31, 2020	Z-0079-2021	—	terminated	Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient
Jan 10, 2020	Z-1380-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1375-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1383-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1370-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1374-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1371-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1366-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1369-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1372-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1381-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1386-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1382-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1376-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1368-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1387-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1367-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1379-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1388-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1377-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1384-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1385-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1378-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Jan 10, 2020	Z-1373-2020	—	terminated	Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment
Feb 26, 2019	Z-2143-2019	—	terminated	During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop.
Feb 26, 2019	Z-2142-2019	—	terminated	During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop.
Feb 26, 2019	Z-2141-2019	—	terminated	During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop.
Feb 26, 2019	Z-2144-2019	—	terminated	During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop.
Feb 26, 2019	Z-2140-2019	—	terminated	During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop.
Mar 8, 2017	Z-1701-2017	—	terminated	A single lot of product that potentially has a single part within the lot that does not match the product on the label due to a commingle at the firm supplier
Sep 14, 2016	Z-0835-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0831-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0860-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0849-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0841-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0836-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0846-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0861-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0848-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0854-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0857-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0862-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0847-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0838-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0842-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0830-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0844-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0845-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0856-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0855-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0851-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0852-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0850-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0829-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0853-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0834-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0859-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0833-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0840-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0828-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0843-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0837-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0863-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0839-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0832-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Sep 14, 2016	Z-0858-2017	—	terminated	A limited number of product pouches may not have been sealed during packaging.
Aug 8, 2016	Z-2845-2016	—	terminated	Product was incorrectly packaged.
Nov 25, 2015	Z-2481-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2410-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2466-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2454-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2522-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2471-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2461-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2415-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2487-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2449-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2465-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2445-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2420-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2470-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2456-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2463-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2479-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2477-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2423-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2427-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2434-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2516-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2519-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2441-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2417-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2408-2016	—	terminated	Pouches may not have been sealed during packing.
Nov 25, 2015	Z-2426-2016	—	terminated	Pouches may not have been sealed during packing.