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Compression Stocking 103

by Gottfried Medical, Inc. 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG4201031 UDI-DI Date4 Jun 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Compression Stocking
Generic Name
Compression/pressure sock/stocking, reusable
Model / Ref / Catalog
103
Primary DI / UDI-DI
G4201031
510(k) Number
FDA Product Code
DWL, FQL
GMDN Term
Compression/pressure sock/stocking, reusable
Device Class
Class II
Regulation Number
880.5780
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K823737)

Show all (12)

Other devices from Gottfried Medical, Inc.

See all devices from Gottfried Medical, Inc. →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No