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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 36 of 37

Device	Model / Reference	Registries	Class	Status
BioHorizons	CNTNA	FDA UDI	Class II	Active
BioHorizons	SGAA	FDA UDI	Class II	Active
BioHorizons	PADS19	FDA UDI	Class I	Active
BioHorizons	TP3ODS6	FDA UDI	Class II	Active
BioHorizons	PROBLGY	FDA UDI	Class I	Active
BioHorizons	PBBA3	FDA UDI	Class II	Active
BioHorizons	122-800	FDA UDI	Class I	Unknown
BioHorizons	CNTBI	FDA UDI	Class II	Active
BioHorizons	PBCMAV	FDA UDI	Class II	Unknown
BioHorizons	MDLTICOZ	FDA UDI	Class II	Active
BioHorizons	BC2259.3320	FDA UDI	Class II	Active
BioHorizons	PBH5009	FDA UDI	Class II	Unknown
BioHorizons	TP3SEA3	FDA UDI	Class II	Active
BioHorizons	BC2259.4320	FDA UDI	Class II	Active
BioHorizons	TRX5809	FDA UDI	Class II	Active
BioHorizons	TMR5807	FDA UDI	Class II	Active
BioHorizons	CC-GY-H	FDA UDI	Class II	Active
BioHorizons	PBCAH	FDA UDI	Class II	Active
BioHorizons	CRHA6	FDA UDI	Class II	Active
BioHorizons	MLW3013Z	FDA UDI	Class II	Active
BioHorizons	HA-YW-R5	FDA UDI	Class II	Active
BioHorizons	PGMU3	FDA UDI	Class II	Active
BioHorizons	PBAFS1	FDA UDI	Class II	Active
BioHorizons	LPBR5015	FDA UDI	Class II	Unknown
BioHorizons	PYODSK5	FDA UDI	Class II	Active
BioHorizons	CA-YW-S	FDA UDI	Class II	Active
BioHorizons	D2015Z	FDA UDI	Class I	Active
BioHorizons	PROIDGY	FDA UDI	Class I	Active
BioHorizons	PXAS	FDA UDI	Class II	Active
BioHorizons	PGCMAV	FDA UDI	Class II	Unknown
BioHorizons	MBAS	FDA UDI	Class I	Active
BioHorizons	PYCTA1	FDA UDI	Class II	Unknown
BioHorizons	MU-GY-304	FDA UDI	Class II	Active
BioHorizons	CRHA4	FDA UDI	Class II	Active
BioHorizons	1022/2905	FDA UDI	Class II	Unknown
BioHorizons	20042	FDA UDI	Class II	Active
BioHorizons	BTR4612	FDA UDI	Class II	Active
BioHorizons	TLX3418	FDA UDI	Class II	Active
BioHorizons	TP3ODS3	FDA UDI	Class II	Active
BioHorizons	PGNHA2	FDA UDI	Class II	Active
BioHorizons	2622	FDA UDI	Class I	Active
BioHorizons	TST2038	FDA UDI	Class I	Active
BioHorizons	TIMD8009XT	FDA UDI	Class I	Active
BioHorizons	CRTBI	FDA UDI	Class II	Active
BioHorizons	PYDBP	EUDAMEDFDA UDI	Class I	Active
BioHorizons	WCAZ	FDA UDI	Class II	Active
The Maestro System 3.0mm Diameter Implant	K032351	FDA 510(k)	Class II	Active
Multi-unit Abutments for CONELOG	K203252	FDA 510(k)	Class II	Active
O-Ring Abutment	K990277	FDA 510(k)	Class II	Active
The Maestro System	K972313	FDA 510(k)	Class II	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.