Identity
- Trade Name
- Avalon Biomed NeoSolv FDA UDI
- Generic Name
- Root canal cleaning solution FDA UDI
- Device Name
- Avalon Biomed NeoSolv - 4 oz Bottle FDA UDI
- Model / Reference
- ABNS4 FDA UDI
- Description
- Avalon Biomed NeoSolv - 4 oz Bottle FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810118106415 FDA UDI
- FDA Product Code
- KJJ FDA UDI
- GMDN Term
- Root canal cleaning solution FDA UDI
Classification
- Device Class
- U 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
No
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
Category: Root canal cleaning solution
Avalon Biomed NeoSolv by Nusmile, Ltd — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- Nusmile, Ltd
Sources (1)
- FDA UDI 67909d82-d05b-49a8-a401-272164b5d97e 33 fields · synced Jun 1, 2026