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Penlon 408001016

by Penlon, Ltd.

Penlon 408001016 is a Class I device made by Penlon, Ltd., listed in FDA GUDID since 6 Dec 2024 (UDI-DI 05051977003728), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05051977003728 UDI-DI Date6 Dec 2024ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Penlon
Generic name
Laryngoscope blade, reusable
Model / Ref / Catalog
408001016
Primary DI / UDI-DI
05051977003728
FDA product code
CCW
GMDN term
Laryngoscope blade, reusable
Device class
Class I
Regulation number
868.5540
GUDID distribution status
Not in Commercial Distribution
MRI safety
MR Safe

Related devices

Category: Laryngoscope blade, reusable

Similar devices in this category

Other devices filed under Laryngoscope blade, reusable.

Other devices from Penlon, Ltd.

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Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)