Identity
- Trade Name
- Precedent FDA UDI
- Generic Name
- Glass ionomer dental cement FDA UDI
- Device Name
- Precedent® is intended for use as an orthodontic band cement. Kit contains: 15g Precedent® Powder, 15g Precedent® Liquid, Spatulas, Scoop, Mixing Pad. FDA UDI
- Model / Reference
- PRS FDA UDI
- Description
- Precedent® is intended for use as an orthodontic band cement. Kit contains: 15g Precedent® Powder, 15g Precedent® Liquid, Spatulas, Scoop, Mixing Pad. FDA UDI
Identifiers
- Catalog Number
- PRS FDA UDI
- Primary DI / UDI-DI
- D798PRS0 FDA UDI
- 510(k) Number
- K934405 FDA UDI
- FDA Product Code
- DYH FDA UDI
- GMDN Term
- Glass ionomer dental cement FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3750 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Glass ionomer dental cement
Precedent by Reliance Orthodontic Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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 II | Pending data |
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Manufacturer
- Manufacturer
- Reliance Orthodontic Products, Inc.
Sources (1)
- FDA UDI b5dd9c63-5173-4fc5-94cc-1bacaaa058c4 37 fields · synced May 30, 2026