Identity
- Trade Name
- DENTECH FDA UDI
- Generic Name
- Hand-held dental retractor FDA UDI
- Device Name
- Retro Filling Retractor FDA UDI
- Model / Reference
- 30600600 FDA UDI
- Description
- Retro Filling Retractor FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04560218680129 FDA UDI
- FDA Product Code
- EIF FDA UDI
- GMDN Term
- Hand-held dental retractor 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Hand-held dental retractor
Dentech by Dentech Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hand-held dental retractor.
- Power Dental USA — Power Dental USA, Inc. · Class I
- Tatum Sinus Retractor — SUNCOAST DENTAL, INC. · Class I
- devemed — devemed GmbH · Class I
- ACE — ACE SURGICAL SUPPLY CO., INC. · Class I
- ACE — ACE SURGICAL SUPPLY CO., INC. · Class I
- ACE — ACE SURGICAL SUPPLY CO., INC. · Class I
- STOMA® — Storz am Mark GmbH · Class I
- DIOnavi. Scan Retractor Lower jaw — DIO Corporation · 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
- Dentech Corp.
Sources (1)
- FDA UDI d64d89ee-64b5-474f-bde0-1e8d65c6018b 33 fields · synced May 30, 2026