Identity
- Trade Name
- OsteoMed FDA UDI
- Generic Name
- Craniofacial fixation plate, non-bioabsorbable, non-customized FDA UDI
- Device Name
- 23mm Left "L" Plate, Sterile FDA UDI
- Model / Reference
- 210-0016-SP FDA UDI
- Description
- 23mm Left "L" Plate, Sterile FDA UDI
Identifiers
- Catalog Number
- 210-0016-SP FDA UDI
- Primary DI / UDI-DI
- 00845694029551 FDA UDI
- FDA Product Code
- DZL FDA UDI
- GMDN Term
- Craniofacial fixation plate, non-bioabsorbable, non-customized FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.4880 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
Dimensions & Sizes
- Size
- Length — 23 Millimeter FDA UDI
Category: Craniofacial fixation plate, non-bioabsorbable, non-customized
OsteoMed by Osteomed Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Craniofacial fixation plate, non-bioabsorbable, non-customized.
- LEVEL ONE CMF — KLS-Martin L.P. · Class II
- Leforte System Bone Plate — Jeil Medical Corporation · Class II
- CMF VISIONARE — VISIONARE LLC · Class II
- MCI - Medical Concept Innovation, Inc. — MCI MEDICAL CONCEPT INNOVATION INC. · Class II
- TraumaOne SYSTEM — BIOMET MICROFIXATION, INC · Class II
- Leforte System Bone Plate — Jeil Medical Corporation · Class II
- AccuPlate® Patient-Specific Plate — Medcad · Class II
- Leforte Neuro System Bone Plate — Jeil Medical Corporation · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Osteomed Corp.
Sources (1)
- FDA UDI 046475c5-20b5-4ae4-8040-858169a7ec43 37 fields · synced May 31, 2026