Identity
- Trade Name
- Innomed, Inc. FDA UDI
- Generic Name
- Orthopaedic surgical distractor, external FDA UDI
- Device Name
- Small Bone Compressor/Distractor 1/16" with Rotating Arms, Driver & Case FDA UDI
- Model / Reference
- 1825-01 FDA UDI
- Description
- Small Bone Compressor/Distractor 1/16" with Rotating Arms, Driver & Case FDA UDI
Identifiers
- Catalog Number
- 1825-01 FDA UDI
- Primary DI / UDI-DI
- 00840277102218 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Orthopaedic surgical distractor, external FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
No
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
No
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: Orthopaedic surgical distractor, external
Innomed, Inc. by Innomed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Arthrex® — Arthrex, Inc. · Class I
- In2Bones — In2Bones, USA · 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 |
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Manufacturer
- Manufacturer
- Innomed, Inc.
Sources (1)
- FDA UDI 5f648d0d-8d71-4b7e-9276-ec6b2c71617c 34 fields · synced May 31, 2026