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BIOHORIZONS IMPLANT SYSTEMS INC.

United States·US-MF-000014002

Last updated September 17, 2026

What BIOHORIZONS IMPLANT SYSTEMS INC. makes

BioHorizons Implant Systems Inc. manufactures dental implant suprastructures, both permanent and temporary preformed types, as well as two-piece screw endosteal dental implants. The company also produces reusable and single-use dental drill bits, resilient dental precision attachments, reusable dental implantation depth/angle gauges, and reusable surgical screwdrivers.

The devices are classified as Class I and Class II medical devices and are listed in the EUDAMED and FDA UDI registries. The company 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 BioHorizons Implant Systems Inc. make?

Where is BioHorizons Implant Systems Inc. based?

BioHorizons Implant Systems Inc. is based in the United States, as stated in the provided device data under the COUNTRY field.

Which registries list BioHorizons Implant Systems Inc.'s devices?

The devices manufactured by BioHorizons Implant Systems Inc. are listed in the EUDAMED and FDA UDI registries, as indicated in the LISTED IN field of the device data.

How are BioHorizons Implant Systems Inc.'s devices classified?

The devices manufactured by BioHorizons Implant Systems Inc. are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field in the provided data.

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

Information

Country: United States
Address: 2300, Riverchase Center, Birmingham, United States
Website: www.biohorizons.com/
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1 (205) 968-7994
PRRC Contact: Jared Cooper
EUDAMED SRN: US-MF-000014002
FDA FEI Number: 1000592496
DUNS Number: —

Catalogue (1836)

Page 28 of 37

Device	Model / Reference	Registries	Class	Status
BioHorizons	CTA5212	FDA UDI	Class II	Active
BioHorizons	PROLD3707	FDA UDI	Class I	Active
BioHorizons	CRIDH	FDA UDI	Class I	Active
BioHorizons	TLXP4609	FDA UDI	Class II	Active
BioHorizons	PBODS5	FDA UDI	Class II	Active
BioHorizons	PGSEA3	FDA UDI	Class II	Active
BioHorizons	PXMUPSA25	FDA UDI	Class II	Active
BioHorizons	TIMD8010XT	FDA UDI	Class I	Active
BioHorizons	TP3HYB2	FDA UDI	Class II	Active
BioHorizons	PYREA	FDA UDI	Class II	Active
BioHorizons	CR20A1W	FDA UDI	Class II	Active
BioHorizons	BC2258.3330	FDA UDI	Class II	Active
BioHorizons	PGNSC	FDA UDI	Class I	Active
BioHorizons	3515D3	FDA UDI	Class II	Unknown
BioHorizons	CMUAS	FDA UDI	Class II	Active
BioHorizons	BSCSZ	FDA UDI	Class I	Active
BioHorizons	TSD2032HDSU	EUDAMEDFDA UDI	Class I	Active
BioHorizons	TP3CMA	FDA UDI	Class II	Active
BioHorizons	PBSSHP2T	FDA UDI	Class II	Active
BioHorizons	PBODSK4	FDA UDI	Class II	Active
BioHorizons	PBRSC	FDA UDI	Class I	Active
BioHorizons	CBDRL	FDA UDI	Class I	Active
BioHorizons	TRX4610	FDA UDI	Class II	Active
BioHorizons	TLX5810	FDA UDI	Class II	Active
BioHorizons	TTLB5810	FDA UDI	Class II	Active
BioHorizons	TP3HYB	FDA UDI	Class II	Active
BioHorizons	TLX4618	FDA UDI	Class II	Active
BioHorizons	SGCD40	FDA UDI	Class I	Unknown
BioHorizons	TP3SSEA3	FDA UDI	Class II	Unknown
BioHorizons	CGS-2524SU	FDA UDI	Class I	Active
BioHorizons	ODS-CAK	FDA UDI	Class I	Active
BioHorizons	TLR3809	FDA UDI	Class II	Active
BioHorizons	ODS-BS	FDA UDI	Class I	Active
BioHorizons	MU-PSS	FDA UDI	Class II	Active
BioHorizons	BTA4610	FDA UDI	Class II	Active
BioHorizons	SYPWSC	FDA UDI	Class I	Active
BioHorizons	PBODS3	FDA UDI	Class II	Active
BioHorizons	233-210	FDA UDI	Class II	Active
BioHorizons	SGHA20	FDA UDI	Class II	Active
BioHorizons	CTA3815R	FDA UDI	Class II	Active
BioHorizons	CA-GY-S3	FDA UDI	Class II	Active
BioHorizons	CTR3810R	FDA UDI	Class II	Active
BioHorizons	TSD4020HD	FDA UDI	Class I	Active
BioHorizons	CGS-5421SU	FDA UDI	Class I	Active
BioHorizons	PGODS0	FDA UDI	Class II	Active
BioHorizons	BTA3815	FDA UDI	Class II	Active
BioHorizons	MDLMWZ	FDA UDI	Class I	Active
BioHorizons	BTD3210	FDA UDI	Class I	Unknown
BioHorizons	PYH3509	FDA UDI	Class II	Unknown
BioHorizons	TP3BAA	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 (6)

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

There are 6 recall records for BioHorizons Implant Systems Inc., with the earliest initiated on September 7, 2010, and the most recent initiated on October 30, 2015. All records are listed with a status of terminated. The reasons given include insufficient cleaning instructions to remove residual contaminants after surgical use, an incorrect stainless steel drill component packaged in place of the correct titanium component in the Tapered HD Upgrade set, a body length discrepancy where the External Implant 40105D3 Lot 1302762 labeled as 10.5mm is actually 12mm, an incorrect label reading 10.5mm instead of the specified 15mm on implant inner vial packaging, and a healing abutment that may not fully seat on the implant.

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
Oct 30, 2015	Z-0391-2016	—	terminated	An incorrect label reading 10.5mm and not the specified 15mm was placed on the implant inner vial packaging.
Apr 16, 2015	Z-1605-2015	—	terminated	BioHorizons Tapered HD Upgrade set was packaged with an incorrect drill component manufactured of stainless steel in place of the correct component manufactured from titanium.
Dec 10, 2013	Z-1058-2014	—	terminated	The body length of the External Implant 40105D3 Lot 1302762 labeled as 10.5mm in length is in fact 12mm in length.
Nov 19, 2012	Z-0561-2013	—	terminated	The cleaning instructions provided may not be sufficient to remove residual contaminants after surgical use.
Nov 19, 2012	Z-0562-2013	—	terminated	The cleaning instructions provided may not be sufficient to remove residual contaminants after surgical use.
Sep 7, 2010	Z-0321-2011	—	terminated	Healing abutment may not fully seat on the implant.