Identity
- Trade Name
- RejuvaKnee FDA UDI
- Generic Name
- Meniscus biomatrix implant, animal-derived FDA UDI
- Device Name
- Collagen Meniscus Implant FDA UDI
- Model / Reference
- REJ075 FDA UDI
- Description
- Collagen Meniscus Implant FDA UDI
Identifiers
- Catalog Number
- REJ075 FDA UDI
- Primary DI / UDI-DI
- 00813954026022 FDA UDI
- FDA Product Code
- OLC FDA UDI
- GMDN Term
- Meniscus biomatrix implant, animal-derived FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Category: Meniscus biomatrix implant, animal-derived
RejuvaKnee by Collagen Matrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Meniscus biomatrix implant, animal-derived.
- RejuvaKnee — COLLAGEN MATRIX, INC. · Class II
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 |
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Manufacturer
- Manufacturer
- Collagen Matrix, Inc.
Sources (1)
- FDA UDI ae3e8571-5eef-4d20-88d1-f0bd87f64efc 37 fields · synced Jun 8, 2026