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GreenLight™ 4558GSP

by Airlife, Inc. 2 variants

GreenLight™ 4558GSP is a Class I device made by Airlife, Inc., listed in FDA GUDID since 27 Feb 2025 (UDI-DI 10889483583937), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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 Number10889483583937 UDI-DI Date27 Feb 2025ListedStatusListed GUDID: 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  • Withdrawn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
GreenLight™
Generic name
Laryngoscope handle, reusable
Model / Ref / Catalog
4558GSP
Primary DI / UDI-DI
10889483583937
FDA product code
CCW
GMDN term
Laryngoscope handle, reusable
Device class
Class I
Regulation number
868.5540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laryngoscope handle, reusable

Similar devices in this category

Other devices filed under Laryngoscope handle, reusable.

Other devices from Airlife, Inc.

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Properties

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