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Axiom SP Visco

by Ki Mobility, LLC 27 variants

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

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 Number00840363371153 UDI-DI Date2 Dec 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Axiom
Generic Name
Wheelchair seat cushion
Model / Ref / Catalog
Axiom SP Visco, XSP1715VIC
Primary DI / UDI-DI
00840363371153
FDA Product Code
IMP
GMDN Term
Wheelchair seat cushion
Device Class
Class I
Regulation Number
890.3920
GUDID distribution status
In Commercial Distribution

Other devices from Ki Mobility, LLC

See all devices from Ki Mobility, LLC →

Properties

  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No