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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 3 of 500

Device	Model / Reference	Registries	Class	Status
Ring Retainer	31-423747	FDA UDI	Class I	Active
Oxford Lateral Instruments	32-423340	FDA UDI	Class II	Active
Optilock	22414	FDA UDI	Class II	Active
Explor	11-210042	FDA UDI	Class II	Active
Taperloc® Lateralized Offset	31-478050	FDA UDI	Class I	Active
M2a Hip System	15-105058	FDA UDI	Class II	Active
Mallory/Head Calcar Hip System	11-104936	FDA UDI	Class II	Active
Integral 180 Hip System	166013	FDA UDI	Class II	Active
RingLoc® Hip System	EP-156233	FDA UDI	Class II	Active
Arcos Modular Revision System	31-301817	FDA UDI	Class II	Active
Oss	32-472106	FDA UDI	Class I	Active
Vanguard(tm)	32-488265	FDA UDI	Class II	Active
Trauma Fixation Systems	27-362422	FDA UDI	Class II	Active
Taperloc Hip System	11-103202	FDA UDI	Class II	Active
Arcos Modular Revision Hip System	11-302024	FDA UDI	Class II	Active
Finn Knee System	153808	FDA UDI	Class II	Active
Ptn Peritrochanteric Nail	29283	FDA UDI	Class II	Active
Regenerex Ringloc + Hip System	PT-104052	FDA UDI	Class II	Active
Maestro(tm) Total Wrist	409182	FDA UDI	Class I	Active
Copeland Humeral Surface Cutter	402622	FDA UDI	Class I	Active
Reunite Screw System	348441	FDA UDI	Class II	Active
Vanguard(tm)	32-484188	FDA UDI	Class I	Active
Oss(tm) Bowed Im Stem Trial	32-472020	FDA UDI	Class I	Active
Ascent Knee System	179116	FDA UDI	Class II	Active
Bi-Metric Hip System	162961	FDA UDI	Class II	Active
Vanguard XP® Instrumentation	32-700202	FDA UDI	Class II	Active
Cannulated Screw	110007767	FDA UDI	Class II	Active
Biomet® Knee System	11-150856	FDA UDI	Class II	Active
Cannulated Screw8.0mm X 130mm (full Thread)	110008038	FDA UDI	Class II	Active
Drill-Tap With T-Handle	25-012	FDA UDI	Class I	Active
Lock Anatomic Fibula Plate Tray	8299-53-016	FDA UDI	Class I	Active
Vanguard 5-In-1 Trial Bearing	32-483600	FDA UDI	Class II	Active
Bmp Cable System	350807	FDA UDI	Class II	Active
Hi-Wall Ringloc® Screw-In	31-195238	FDA UDI	Class I	Active
Signature Instrumentation	110004347	FDA UDI	Class II	Active
Arcos Modular Revision Hip System	11-300913	FDA UDI	Class II	Active
OSS™ Orthopedic Salvage System	161076	FDA UDI	Class II	Active
Cancellous Locking Screw	8161-40-065	FDA UDI	Class II	Active
Vanguard®	32-487023	FDA UDI	Class I	Active
Polyaxlocking Cortical Screw Full Thread	8150-45-534	FDA UDI	Class II	Active
Cortical Bone Screw	14377-48	FDA UDI	Class II	Active
Bio-Moore Endo Ii Hip System	12-139036	FDA UDI	Class II	Active
Ringloc Hip System	12-105995	FDA UDI	Class II	Active
Ezloc(tm) Depth Gauge	904761	FDA UDI	Class I	Active
RingLoc Hip System	EP-105928	FDA UDI	Class II	Active
Repicci Ii Resurfacing Knee System	215065	FDA UDI	Class II	Active
Taperloc Hip System	21-123207	FDA UDI	Class II	Active
Phoenix Nail System	14-443024	FDA UDI	Class II	Active
Vanguard Xp	32-700002	FDA UDI	Class I	Active
Leg Positioner Pad, 2 Pk	905039	FDA UDI	Class I	Active

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