Identity
- Trade Name
- EXTRACTION FORCEPS #36A FDA UDI
- Generic Name
- Tooth extraction forceps FDA UDI
- Model / Reference
- 10-0500-036A FDA UDI
Identifiers
- Primary DI / UDI-DI
- D928100500036A0 FDA UDI
- FDA Product Code
- EMG FDA UDI
- GMDN Term
- Tooth extraction forceps 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Tooth extraction forceps
Extraction Forceps #36a by W.H. Holden, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tooth extraction forceps.
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- Premier Forceps — PREMIER DENTAL PRODUCTS COMPANY · Class I
- Henry Schein — HENRY SCHEIN, INC. · Class I
- A. Titan Instruments — A.Titan Instruments · Class I
- devemed — devemed GmbH · Class I
- Power Dental USA — Power Dental USA, Inc. · Class I
- NORDENT MANUFACTURING INC — NORDENT MANUFACTURING INC · Class I
- ZOLL-DENTAL — Zoll-Dental · 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 |
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Manufacturer
- Manufacturer
- W.H. Holden, Inc.
Sources (1)
- FDA UDI bc1d3621-fa12-46bb-9304-24545f28340c 32 fields · synced Jun 8, 2026