Tanda Series 4
by Tanda Beauty Canada, Inc 3 variants
Tanda Series 4 (HU-FG00631) is a red/blue light phototherapy unit (FDA Class II; FDA product code GEX, Powered Laser Surgical Instrument) made by Tanda Beauty Canada, Inc, cleared under FDA 510(k) K080591 on 14 Nov 2008 and listed in FDA GUDID since 2 Oct 2017 (UDI-DI 00806248004936), 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 | Number00806248004936 | Date2 Oct 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK080591 | Date14 Nov 2008 | StatusActive |
Official records
- AccessGUDID record 00806248004936
- FDA 510(k) database K080591
Across registries
- FDA 510(k) K080591 decided 14 Nov 2008 Active
- FDA GUDID UDI-DI 00806248004936 listed 2 Oct 2017 Listed
Timeline
- Cleared FDA 510(k) K080591
- Listed FDA GUDID 00806248004936
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Tanda
- Generic name
- Red/blue light phototherapy unit
- Model / Ref / Catalog
- Series 4, HU-FG00631
- Primary DI / UDI-DI
- 00806248004936
- 510(k) Number
- FDA product code
- GEX
- GMDN term
- Red/blue light phototherapy unit
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
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