Identity
- Trade Name
- PRO FDA UDI
- Generic Name
- Bone approximation clamp FDA UDI
- Device Name
- Jaw Clamp FDA UDI
- Model / Reference
- 705452 FDA UDI
- Description
- Jaw Clamp FDA UDI
Identifiers
- Catalog Number
- 705452 FDA UDI
- Primary DI / UDI-DI
- 07613327131826 FDA UDI
- FDA Product Code
- HXD FDA UDI
- GMDN Term
- Bone approximation clamp FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
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: Bone approximation clamp
Pro by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone approximation clamp.
- Journey II — Smith & Nephew, Inc. · Class II
- PERI-LOC VLP — Smith & Nephew, Inc. · Class II
- LEGION — Smith & Nephew, Inc. · Class I
- Bone Clamp — Koros USA, Inc. · Class I
- PROFIX — Smith & Nephew, Inc. · Class II
- Sklar® — Sklar Corporation · Class I
- BOSS Instruments — Boss Instruments, Ltd. · Class I
- Symmetry Martin — SYMMETRY SURGICAL INC. · Class I
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 333d543b-9538-4719-86a4-6047ebe39fde 34 fields · synced Jun 1, 2026