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Supracor Stumulite Honeycomb SP2019

by Supracor, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842749110547 UDI-DIDate14 Sep 2023ListedStatusListed GUDID: not 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  • Withdrawn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 22 Oct 2026.

Specification

GUDID

Trade Name
Supracor Stumulite Honeycomb
Generic Name
Wheelchair seat cushion
Model / Reference
SP2019
Primary DI / UDI-DI
00842749110547
FDA Product Code
IMP
GMDN Term
Wheelchair seat cushion
Device Class
Class I
Regulation Number
890.3920
GUDID distribution status
Not in Commercial Distribution

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • 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