← Back to catalogue
Dual-Force™ Sectional Matrix System Complete Kit w/Ultra-Wrap
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Dual-Force™ Sectional Matrix System Complete Kit w/Ultra-Wrap FDA UDI
- Generic Name
- Dental matrix band kit FDA UDI
- Device Name
- Collection of devices for direct restoration procedures FDA UDI
- Model / Reference
- 209022 FDA UDI
- Description
- Collection of devices for direct restoration procedures FDA UDI
Identifiers
- Catalog Number
- 209022 FDA UDI
- Primary DI / UDI-DI
- 00359883004408 FDA UDI
- FDA Product Code
- DZN FDA UDI
- GMDN Term
- Dental matrix band kit 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental matrix band kit
Dual-Force™ Sectional Matrix System Complete Kit w/Ultra-Wrap by Den-Mat Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental matrix band kit.
- Composi-Tight® — GARRISON DENTAL SOLUTIONS, L.L.C. · Class I
- NiTin Garrison® — GARRISON DENTAL SOLUTIONS, L.L.C. · Class I
- Premier X5 Sectional Matrix System — PREMIER DENTAL PRODUCTS COMPANY · Class I
- HD Anterior Matrix Kit — Bioclear Matrix Systems, LLC
- Composi-Tight® — GARRISON DENTAL SOLUTIONS, L.L.C. · Class I
- eZr™ — GARRISON DENTAL SOLUTIONS, L.L.C. · Class I
- Dual-Force™ Sectional Matrix System Starter Kit w/ Ultra-Wrap — CLINICIAN'S CHOICE DENTAL PRODUCTS, INC. · Class I
- Plasdent — PLASDENT CORP. · 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
- Den-Mat Holdings, LLC
Sources (1)
- FDA UDI 38dcd399-6f40-4813-b4e9-e88195bb9fc3 36 fields · synced Jun 9, 2026