Belcypher-N
Belcypher-N is a Class II device made by Takara Belmont Corp., cleared under FDA 510(k) K110160 on 17 Feb 2011 and listed in FDA GUDID since 21 Sep 2016 (UDI-DI 04560217093692), active as of 21 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 | Number04560217093692 | Date21 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK110160 | Date17 Feb 2011 | StatusActive |
Official records
- AccessGUDID record 04560217093692
- FDA 510(k) database K110160
Across registries
- FDA 510(k) K110160 decided 17 Feb 2011 Active
- FDA GUDID UDI-DI 04560217093692 listed 21 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K110160
- Listed FDA GUDID 04560217093692
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Stationary panoramic dental x-ray system, digital
- Model / Ref / Catalog
- BELCYPHER, BELCYPHER-N
- Primary DI / UDI-DI
- 04560217093692
- 510(k) Number
- FDA product code
- MUH
- GMDN term
- Stationary panoramic dental x-ray system, digital
- Device class
- Class II
- Regulation number
- 872.1800
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Stationary panoramic dental x-ray system, digital.