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Convaid Reno 16

by Convaid Products LLC

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 Number00840117408685 UDI-DI Date5 Mar 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  • Withdrawn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
Convaid
Generic Name
Attendant-only-propelled wheelchair, non-bariatric
Model / Ref / Catalog
Reno 16, 905500
Primary DI / UDI-DI
00840117408685
510(k) Number
FDA Product Code
IOR
GMDN Term
Attendant-only-propelled wheelchair, non-bariatric
Device Class
Class I
Regulation Number
890.3850
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K032402)

Other devices from Convaid Products LLC

See all devices from Convaid Products LLC →

Properties

  • Serial Number
  • Manufacturing Date

Other properties (12)

  • 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
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No