Identity
- Trade Name
- NORDENT MANUFACTURING INC FDA UDI
- Generic Name
- Dental articulation paper forceps FDA UDI
- Device Name
- EXTRC FCP LWR MLR STR HDL #22 FDA UDI
- Model / Reference
- FE22 FDA UDI
- Description
- EXTRC FCP LWR MLR STR HDL #22 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840018643925 FDA UDI
- FDA Product Code
- HTD FDA UDI
- GMDN Term
- Dental articulation paper forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Category: Dental articulation paper forceps
Nordent Manufacturing Inc by Nordent Manufacturing Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental articulation paper forceps.
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- J&J Instruments — J&J Instruments, LLC · Class I
- Henry Schein — HENRY SCHEIN, INC. · Class I
- Henry Schein — HENRY SCHEIN, INC. · Class I
- BENCO — BENCO DENTAL SUPPLY CO. · Class I
- Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLC · Class I
- J&J Instruments — J&J Instruments, LLC · 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
- Nordent Manufacturing Inc
Sources (1)
- FDA UDI 8cbe7f46-4e88-4361-8ed4-9bbcf62821cc 33 fields · synced May 31, 2026