NovaPro Flow 61215-211
NovaPro Flow 61215-211 is a Class II device made by Nanova Biomaterials Inc, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 10816537020209), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10816537020209 | Date16 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 10816537020209
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- NovaPro Flow
- Generic name
- Dental composite resin
- Model / Ref / Catalog
- 61215-211
- Primary DI / UDI-DI
- 10816537020209
- FDA product code
- EBF
- GMDN term
- Dental composite resin
- Device class
- Class II
- Regulation number
- 872.3690
- GUDID distribution status
- In Commercial Distribution
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