MiniFESS LP100
MiniFESS LP100 (IS-100) is a Class I device made by Stryker Corp., listed in FDA GUDID since 3 Sep 2020 (UDI-DI 00857326005154), 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 | Number00857326005154 | Date3 Sep 2020 | StatusListed |
Official records
- AccessGUDID record 00857326005154
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- MiniFESS
- Generic name
- ENT transilluminator
- Model / Ref / Catalog
- LP100, IS-100
- Primary DI / UDI-DI
- 00857326005154
- FDA product code
- LRC
- GMDN term
- ENT transilluminator
- Device class
- Class I
- Regulation number
- 874.4420
- GUDID distribution status
- In Commercial Distribution
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