Identity
- Trade Name
- Power Dental U.S.A., Inc. FDA UDI
- Generic Name
- Dental surgical probe, reusable FDA UDI
- Device Name
- EXP 23 S/E, 1EZ, ENGRAVE 20-EXP 23 FDA UDI
- Model / Reference
- NMM1005 FDA UDI
- Description
- EXP 23 S/E, 1EZ, ENGRAVE 20-EXP 23 FDA UDI
Identifiers
- Catalog Number
- NMM1005 FDA UDI
- Primary DI / UDI-DI
- D943NMM1005 FDA UDI
- FDA Product Code
- EKB FDA UDI
- GMDN Term
- Dental surgical probe, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- Not 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
Power Dental U.S.A., Inc. by Power Dental USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Power Dental USA, Inc.
Sources (1)
- FDA UDI 879d187d-f3c8-41b3-b81b-a3beb3977c6d 36 fields · synced May 31, 2026