Identity
- Trade Name
- FenderMate FDA UDI
- Generic Name
- Dental wedge, single-use FDA UDI
- Model / Reference
- Prime Long FDA UDI
Identifiers
- Catalog Number
- 602817 FDA UDI
- Primary DI / UDI-DI
- 17310236028175 FDA UDI
- FDA Product Code
- JEP FDA UDI
- GMDN Term
- Dental wedge, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental wedge, single-use
FenderMate by Directa AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental wedge, single-use.
- Henry Schein — HENRY SCHEIN, INC. · Class I
- Diamond Wedge — Bioclear Matrix Systems, LLC · Class I
- Bioclear Diamond Wedge — Bioclear Matrix Systems, LLC · Class I
- Bioclear Diamond Wedge — Bioclear Matrix Systems, LLC · Class I
- G-Wedge™ — GARRISON DENTAL SOLUTIONS, L.L.C. · Class I
- Bioclear Diamond Wedge — Bioclear Matrix Systems, LLC · Class I
- SoftWedge™ — GARRISON DENTAL SOLUTIONS, L.L.C. · Class I
- Wykle Wedges 17mm Green Color 500 count — WYKLE RESEARCH, INC. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Directa AB
Sources (1)
- FDA UDI 89bf4e2d-2c78-4787-80ae-4dcd7e8cee00 33 fields · synced May 31, 2026