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Quickie Frontier V6

by Sunrise Medical (US) LLC

Quickie Frontier V6 (FrontierV6) is a wheelchair recliner (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Sunrise Medical (US) LLC, cleared under FDA 510(k) K213090 on 19 Nov 2021 and listed in FDA GUDID since 5 Sep 2023 (UDI-DI 00016958059724), active as of 15 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 15 Oct 2026

Documents

510(k) K213090

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 15 Oct 2026.

Regulatory status

as of registry sync 15 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00016958059724 UDI-DI Date5 Sep 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK213090 Date19 Nov 2021DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K213090 decided 19 Nov 2021 Active
  • FDA GUDID UDI-DI 00016958059724 listed 5 Sep 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K213090
  2. Listed FDA GUDID 00016958059724

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Generic name
Wheelchair recliner, battery-powered
Model / Ref / Catalog
Frontier V6, FrontierV6
Primary DI / UDI-DI
00016958059724
510(k) Number
FDA product code
ITI
GMDN term
Wheelchair recliner, battery-powered
Device class
Class II
Regulation number
890.3860
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ITI (Wheelchair, Powered).

Other devices from Sunrise Medical (US) LLC

See all devices from Sunrise Medical (US) LLC →

Properties

  • Over-the-counter
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)