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Penlon 310106

by Penlon, Ltd.

Penlon 310106 is a Class II device made by Penlon, Ltd., listed in FDA GUDID since 12 Sep 2016 (UDI-DI 05051977000277), 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 Number05051977000277 UDI-DI Date12 Sep 2016ListedStatusListed 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  • Withdrawn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
Penlon
Generic name
Vacuum suction regulator/regulation set, general-purpose
Model / Ref / Catalog
310106
Primary DI / UDI-DI
05051977000277
FDA product code
GCX
GMDN term
Vacuum suction regulator/regulation set, general-purpose
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vacuum suction regulator/regulation set, general-purpose

Similar devices

Other devices filed under FDA product code GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered).

Other devices from Penlon, Ltd.

See all devices from Penlon, Ltd. →

Properties

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