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Xtend Foot Fri H100 H100-427-STY-FTR

by C Lindhextend AB GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07350104146139 UDI-DIDate16 Jun 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Xtend Foot Fri H100
Generic Name
Mechanical-resistance external ankle-foot prosthesis
Model / Ref / Catalog
H100-427-STY-FTR
Primary DI / UDI-DI
07350104146139
FDA Product Code
ISH
GMDN Term
Mechanical-resistance external ankle-foot prosthesis
Device Class
Class I
Regulation Number
890.3420
GUDID distribution status
In Commercial Distribution

Other devices from C Lindhextend AB

See all devices from C Lindhextend AB →

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No