Bosidin D-1130
by Shenzhen Bosidin Technology Co., Ltd.
Bosidin D-1130 is a Class II device made by Shenzhen Bosidin Technology Co., Ltd., cleared under FDA 510(k) K192432 on 8 Nov 2019 and listed in FDA GUDID since 10 Jan 2020 (UDI-DI 06970112301309), active as of 22 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 | Number06970112301309 | Date10 Jan 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK192432 | Date8 Nov 2019 | StatusActive |
Official records
- AccessGUDID record 06970112301309
- FDA 510(k) database K192432
Across registries
- FDA 510(k) K192432 decided 8 Nov 2019 Active
- FDA GUDID UDI-DI 06970112301309 listed 10 Jan 2020 Listed
Timeline
- Cleared FDA 510(k) K192432
- Listed FDA GUDID 06970112301309
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Bosidin
- Generic name
- Intense pulsed light skin surface treatment system
- Model / reference
- D-1130
- Primary DI / UDI-DI
- 06970112301309
- 510(k) Number
- FDA product code
- OHT
- GMDN term
- Intense pulsed light skin surface treatment system
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
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