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Biomet Orthopedics, Inc.

United States·US-MF-000001414

Last updated May 23, 2026

What Biomet Orthopedics, Inc. makes

Biomet Orthopedics, Inc. manufactures orthopaedic bone screws that are non-bioabsorbable and available in both sterile and non-sterile forms. The company also produces reusable trial components for acetabulum, knee tibia, and knee femur prostheses, as well as reusable implantation positioning instruments, tibial inserts, and reusable instrument trays. Example devices include the Comprehensive® Shoulder Instruments, TAPERLOC COMPLETE XR 123 MICRO FEMORAL, OSS(TM) RS 7CM SEGMENTAL FEMORAL, Arcos Modular Revision Hip System, VANGUARD SSK 360 KNEE SYSTEM, COMPRESS DEVICE, REPICCI II RESURFACING KNEE SYSTEM, and various Vanguard® Knee System components.

The manufacturer's devices span Class I, Class II, and Class III classifications and are listed in the FDA's Global Unique Device Identification Database (GUDID) under the fda_udi registry. Biomet Orthopedics, Inc. 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 Orthopedics, Inc. manufacture?

Where is Biomet Orthopedics, Inc. based?

Biomet Orthopedics, Inc. is based in the United States. The company operates from its headquarters located in the US, where it designs, manufactures, and distributes its orthopaedic medical devices.

Which registries list Biomet Orthopedics, Inc.'s devices?

Biomet Orthopedics, Inc.'s devices are listed in the FDA's Global Unique Device Identification Database (GUDID) under the fda_udi registry. This database provides public access to device identification information, including the company's orthopaedic implants and instruments.

How are Biomet Orthopedics, Inc.'s devices classified?

Biomet Orthopedics, Inc.'s devices span Class I, Class II, and Class III classifications. Class I devices are low-risk, Class II devices are moderate-risk, and Class III devices are high-risk, with each class subject to different regulatory requirements and controls.

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

Information

Country: United States
Address: 56 , East Bell Drive, Warsaw, United States
Website: labeling.zimmerbiomet.com/
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1 800 348 9500
PRRC Contact: Donnae Abbood
EUDAMED SRN: US-MF-000001414
FDA FEI Number: —
DUNS Number: —

Catalogue (41902)

Page 2 of 500

Device	Model / Reference	Registries	Class	Status
Platform Holder	14645	FDA UDI	Class I	Active
Screw Cortical	1312-12-118	FDA UDI	Class II	Active
Aim™femoral Nail	1014-50	FDA UDI	Class II	Active
Symmetry Plate Module	1940	FDA UDI	Class I	Active
Optilock Periarticular Plating System	26650	FDA UDI	Class II	Active
Biomet Knee System	CP102887	FDA UDI	Class II	Active
Comprehensive® Shoulder System	31-406998	FDA UDI	Class II	Active
Implant Style +5 Ring-Loc	31-103917	FDA UDI	Class I	Active
Taperloc Complete Primary Femoral	51-104150	FDA UDI	Class II	Active
Vanguard®	32-489081	FDA UDI	Class II	Active
Oss Bowed Stem Trial	110018707	FDA UDI	Class II	Active
Ptn Peritrochanteric Nail	29940	FDA UDI	Class II	Active
Affixus®hip Fracture Nail Lag Screw	8145-10-095	FDA UDI	Class II	Active
Oss™	110018803	FDA UDI	Class I	Active
ReCap®	31-500742	FDA UDI	Class I	Active
Arcos® Modular Revision System	31-301804	FDA UDI	Class II	Active
Dvr®	1312-12-009	FDA UDI	Class II	Active
Oss™	595129	FDA UDI	Class I	Active
3.5mm Hex Screw Extractor	14-442084	FDA UDI	Class I	Active
PTN Peritrochanteric Nail	29330	FDA UDI	Class II	Active
0.9mm K-Wire Depth Gauge	110018535	FDA UDI	Class II	Active
Cannulated Screw 4.0mm X 60mm (partial Thread)	110007569	FDA UDI	Class II	Active
Cannulated Cancellous Lag Screw, Reduced Head	1802-53-042	FDA UDI	Class II	Active
Agc Ps Tibial Provisional	32-468150	FDA UDI	Class I	Active
Juggerknot Percutaneous Reusable Trocar	912038P	FDA UDI	Class II	Active
Oss™	CP461009	FDA UDI	Class I	Active
Optilock Periarticular Plating System	26652	FDA UDI	Class II	Active
Ascent Knee Instrumentation	32-379652	FDA UDI	Class I	Active
Protrusio Cage	31-109237	FDA UDI	Class I	Active
Taperloc Hip System	13-103207	FDA UDI	Class II	Active
Bi-Metric Head/Neck Hip System	12-162383	FDA UDI	Class II	Active
Reach Revision Hip System	11-162120	FDA UDI	Class II	Active
Versanail®tibial Nail	1812-10-240	FDA UDI	Class II	Active
Dnp Anatomic Right	DNPAR	FDA UDI	Class II	Active
RingLoc Hip System	EP-105817	FDA UDI	Class II	Active
3.5mm Driver	14505	FDA UDI	Class I	Active
Arcos One-Piece Revision System	11-304024	FDA UDI	Class II	Active
Vanguard Xp	32-700372	FDA UDI	Class I	Active
Ringloc+ Maxrom+ Trial Liner	33-108628	FDA UDI	Class I	Active
Pps Ringloc+ Shell Trials	33-433756	FDA UDI	Class I	Active
Arcos	31-300920	FDA UDI	Class II	Active
Vanguard 360 Revision System	185381	FDA UDI	Class II	Active
Series A	32-486536	FDA UDI	Class I	Active
Arcos Modular Revision Hip System	11-301022	FDA UDI	Class II	Active
Ringloc Hip System	105935	FDA UDI	Class II	Active
Bmp Compression Hip Screw	196160	FDA UDI	Class II	Unknown
Biomet Knee System	141514	FDA UDI	Class II	Active
Solid Hexalobular Driver ZH	110009967	FDA UDI	Class II	Active
A.l.p.s.®	8512-35-075	FDA UDI	Class II	Active
Modular Bio-Core Tap	905052	FDA UDI	Class I	Active

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