Neodent 110315
by JJGC Indústria e Comércio de Materiais Dentários S/A.
Neodent 110315 is a Class II device made by JJGC Indústria e Comércio de Materiais Dentários S/A., cleared under FDA 510(k) K214051 on 13 Apr 2022 and listed in FDA GUDID since 3 May 2022 (UDI-DI 07899878055891), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07899878055891 | Date3 May 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK214051 | Date13 Apr 2022 | StatusActive |
Official records
- AccessGUDID record 07899878055891
- FDA 510(k) database K214051
Across registries
- FDA 510(k) K214051 decided 13 Apr 2022 Active
- FDA GUDID UDI-DI 07899878055891 listed 3 May 2022 Listed
Timeline
- Cleared FDA 510(k) K214051
- Listed FDA GUDID 07899878055891
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Neodent
- Generic name
- Instrument tray, reusable
- Model / Ref / Catalog
- 110315
- Primary DI / UDI-DI
- 07899878055891
- 510(k) Number
- FDA product code
- KCT
- GMDN term
- Instrument tray, reusable
- Device class
- Class II
- Regulation number
- 880.6850
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 195 Millimeter
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