Identity
- Trade Name
- Vanguard® FDA UDI
- Generic Name
- Surgical drill guide, reusable FDA UDI
- Model / Reference
- 32-486534 FDA UDI
Identifiers
- Catalog Number
- 32-486534 FDA UDI
- Primary DI / UDI-DI
- 00887868494949 FDA UDI
- 510(k) Number
- K093293 FDA UDI
- FDA Product Code
- JWH FDA UDIMBV FDA UDI
- GMDN Term
- Surgical drill guide, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical drill guide, reusable
Vanguard® by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical drill guide, reusable.
- ORTHOFIX — Orthofix, Inc. · Class I
- Titan™ — Ascension Orthopedics, Inc. · Class I
- Medtronic Resuable Instruments — MEDTRONIC SOFAMOR DANEK, INC. · Class I
- Distal Elbow Plating System — SKELETAL DYNAMICS L.L.C. · Class II
- Truliant — Exactech, Inc. · Class II
- Vantage — Exactech, Inc. · Class II
- Legion — Smith & Nephew, Inc. · Class II
- Hintermann Series — Dt Medtech, LLC · Class I
Cleared under the same submission
K093293 also covers:
- BIOMET 360 — Biomet Orthopedics, Inc.
- BIOMET 360 KNEE SYSTEM — Biomet Orthopedics, Inc.
- BIOMET 360 KNEE SYSTEM — Biomet Orthopedics, Inc.
- BIOMET 360 KNEE SYSTEM — Biomet Orthopedics, Inc.
- BIOMET 360 KNEE SYSTEM — Biomet Orthopedics, Inc.
- BIOMET KNEE — Biomet Orthopedics, Inc.
- BIOMET® 360 — Biomet Orthopedics, Inc.
- BIOMET® 360 — Biomet Orthopedics, Inc.
- BIOMET® 360 — Biomet Orthopedics, Inc.
- BIOMET® 360 — Biomet Orthopedics, Inc.
- BIOMET® 360 — Biomet Orthopedics, Inc.
- BIOMET® 360 INSTRUMENTS — Biomet Orthopedics, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI fe014fd4-eb95-4ea5-9ef1-eac97d63a50b 36 fields · synced Jun 8, 2026