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PostFree 3105000801

by Stryker Corp.

PostFree 3105000801 (3105-000-801) is a Class I device made by Stryker Corp., listed in FDA GUDID since 31 Aug 2017 (UDI-DI 07613327376340), 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 Number07613327376340 UDI-DI Date31 Aug 2017ListedStatusListed 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  • Withdrawn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
PostFree
Generic name
Traction boot
Model / Ref / Catalog
3105000801, 3105-000-801
Primary DI / UDI-DI
07613327376340
FDA product code
HST
GMDN term
Traction boot
Device class
Class I
Regulation number
888.5850
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HST (Apparatus, traction, non-powered).

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)