Penlon
Penlon is a Class I device made by Penlon, Ltd., listed in FDA GUDID since 21 Jun 2023 (UDI-DI 05051977000765), registry data as of 23 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 | Number05051977000765 | Date21 Jun 2023 | StatusListed |
Official records
- AccessGUDID record 05051977000765
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Laryngoscope blade, reusable
- Model / reference
- ISO ‘Red’ System Premier Fibrelight Blade
- Primary DI / UDI-DI
- 05051977000765
- FDA product code
- CCW
- GMDN term
- Laryngoscope blade, reusable
- Device class
- Class I
- Regulation number
- 868.5540
- GUDID distribution status
- In Commercial Distribution
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