Skip to content

Levo Lae

by LEVO AG Wohlen

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 Number07613045036762 UDI-DI Date9 Sep 2025ListedStatusListed 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  • Withdrawn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
Levo
Generic Name
Push-rim manual wheelchair, non-bariatric
Model / Ref / Catalog
LAE, LAE/L-XL/42/51
Primary DI / UDI-DI
07613045036762
510(k) Number
FDA Product Code
IPL
GMDN Term
Push-rim manual wheelchair, non-bariatric
Device Class
Class II
Regulation Number
890.3900
GUDID distribution status
In Commercial Distribution

Related devices

Category: Push-rim manual wheelchair, non-bariatric

Other devices from LEVO AG Wohlen

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