Pretika ST290
Pretika ST290 is an ultrasonic skin surface treatment unit (FDA Class I) made by Pretika Corporation, listed in FDA GUDID since 30 Apr 2020 (UDI-DI 00813859002909), registry data as of 22 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 | Number00813859002909 | Date30 Apr 2020 | StatusListed |
Official records
- AccessGUDID record 00813859002909
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pretika
- Generic name
- Ultrasonic skin surface treatment unit
- Model / Ref / Catalog
- ST290
- Primary DI / UDI-DI
- 00813859002909
- FDA product code
- ISA, GFE
- GMDN term
- Ultrasonic skin surface treatment unit
- Device class
- Class I
- Regulation number
- 890.5660, 878.4820
- GUDID distribution status
- In Commercial Distribution
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