Identity
- Trade Name
- RELJA Reduction Clamp (Left and Right) FDA UDI
- Generic Name
- Orthopaedic surgical procedure kit, non-medicated, single-use FDA UDI
- Device Name
- The Relja Innovations Reduction Clamp is a manual surgical instrument intended to position and compress the metatarsal joints during an orthopedic surgery. FDA UDI
- Model / Reference
- RI-CC-LR FDA UDI
- Description
- The Relja Innovations Reduction Clamp is a manual surgical instrument intended to position and compress the metatarsal joints during an orthopedic surgery. FDA UDI
Identifiers
- Catalog Number
- RI-CC-LR FDA UDI
- Primary DI / UDI-DI
- 00860005968817 FDA UDI
- FDA Product Code
- HWN FDA UDI
- GMDN Term
- Orthopaedic surgical procedure kit, non-medicated, single-use 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Orthopaedic surgical procedure kit, non-medicated, single-use
RELJA Reduction Clamp (Left and Right) by Relja Innovations, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Relja Innovations, LLC
Sources (1)
- FDA UDI 417180de-394a-4b7c-a452-ab05930266a5 35 fields · synced May 30, 2026