Identity
- Trade Name
- Dual-Force™ Sectional Matrix System Wedge Kit FDA UDI
- Generic Name
- Dental matrix band, single-use FDA UDI
- Device Name
- Double-inclined planes used for separating teeth FDA UDI
- Model / Reference
- 209000 FDA UDI
- Description
- Double-inclined planes used for separating teeth FDA UDI
Identifiers
- Catalog Number
- 209000 FDA UDI
- Primary DI / UDI-DI
- 07540172016902 FDA UDI
- FDA Product Code
- DZN FDA UDI
- GMDN Term
- Dental matrix band, single-use 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
Yes
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
Category: Dental matrix band, single-use
Dual-Force™ Sectional Matrix System Wedge Kit by Clinician's Choice Dental Products, Inc. — Class I — FDA UDI — listed in FDA GUDID
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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
- Clinician's Choice Dental Products, Inc.
Sources (1)
- FDA UDI 3cff6752-214c-411e-a526-a7e7023af764 35 fields · synced May 31, 2026