Identity
- Trade Name
- Chairside FDA UDI
- Generic Name
- Denture reliner, soft, professional FDA UDI
- Device Name
- Chairside Soft Reline Material FDA UDI
- Model / Reference
- 09573 FDA UDI
- Description
- Chairside Soft Reline Material FDA UDI
Identifiers
- Catalog Number
- 09573 FDA UDI
- Primary DI / UDI-DI
- 00840481111778 FDA UDI
- FDA Product Code
- EBI FDA UDI
- GMDN Term
- Denture reliner, soft, professional FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3760 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Weight — 52 Gram FDA UDITotal Volume — 10 Milliliter FDA UDI
Category: Denture reliner, soft, professional
Chairside by Zest Anchors, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Zest Anchors, LLC
Sources (1)
- FDA UDI 13ca3fbe-19a2-4f16-91a7-9e5a9812fed4 37 fields · synced Jun 9, 2026