Identity
- Trade Name
- Plasdent FDA UDI
- Generic Name
- Dental matrix band kit FDA UDI
- Device Name
- Sectional Matrix Kit FDA UDI
- Model / Reference
- MTX-KIT FDA UDI
- Description
- Sectional Matrix Kit FDA UDI
Identifiers
- Catalog Number
- MTX-KIT FDA UDI
- Primary DI / UDI-DI
- D832MTXKIT1 FDA UDI
- FDA Product Code
- NRD FDA UDI
- GMDN Term
- Dental matrix band kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6640 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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 kit
Plasdent by Plasdent Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental matrix band kit.
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- HD Anterior Matrix Kit — Bioclear Matrix Systems, LLC
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- 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
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
- Plasdent Corp.
Sources (1)
- FDA UDI 50be0f6b-342b-4ccd-a6e8-5473eb4e3ea4 34 fields · synced May 30, 2026