Identity
- Trade Name
- FRAGMENT FIXATION SYSTEM FDA UDI
- Generic Name
- Wire cutter FDA UDI
- Device Name
- WIRE CUTTER RE-USE KIT FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- WIRE CUTTER RE-USE KIT FDA UDI
Identifiers
- Catalog Number
- W1004 FDA UDI
- Primary DI / UDI-DI
- 18032568865271 FDA UDI
- 510(k) Number
- K944092 FDA UDI
- FDA Product Code
- JEC FDA UDI
- GMDN Term
- Wire cutter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Width — 156 Millimeter FDA UDI
Category: Wire cutter
Fragment Fixation System by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K944092 also covers:
- FRAGMENT FIXATION SYSTEM — Orthofix, Inc.
- FRAGMENT FIXATION SYSTEM — Orthofix, Inc.
- FRAGMENT FIXATION SYSTEM — Orthofix, Inc.
- Fragment Fixation System — Orthofix, Inc.
- Fragment Fixation System — Orthofix, Inc.
- Fragment Fixation System — Orthofix, Inc.
- Fragment Fixation System — Orthofix, Inc.
- Fragment Fixation System — Orthofix, Inc.
- Fragment Fixation System — Orthofix, Inc.
- Fragment Fixation System — Orthofix, Inc.
- Fragment Fixation System — Orthofix, Inc.
- Fragment Fixation System — Orthofix, 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
- Orthofix, Inc.
Sources (1)
- FDA UDI b6c366a7-8f80-4aaa-9cdf-094606c61dc3 37 fields · synced May 30, 2026