Pops 201
Pops 201 is a Class I device made by Trifecta Therapeutics LLC, listed in FDA GUDID since 9 Sep 2025 (UDI-DI 00860014135408), 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 | Number00860014135408 | Date9 Sep 2025 | StatusListed |
Official records
- AccessGUDID record 00860014135408
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pops
- Generic name
- Skin surface device adhesive
- Model / reference
- 201
- Primary DI / UDI-DI
- 00860014135408
- FDA product code
- KGX
- GMDN term
- Skin surface device adhesive
- Device class
- Class I
- Regulation number
- 880.5240
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
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