510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K010135Substantially Equivalent

Models Lynx and Panther Motorized Scooters, Models Lynx Sx-3, Lynx Sx-3P, Lynx Lx-3, Lynx Lx-3, Panther Lx-4

Invacare GmbH, Elyria OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K010135 is the FDA 510(k) clearance record for MODELS LYNX AND PANTHER MOTORIZED SCOOTERS, MODELS LYNX SX-3, LYNX SX-3P, LYNX LX-3, LYNX LX-3, PANTHER LX-4, a class II device, cleared for Invacare Corp. on under FDA product code INI (Vehicle, Motorized 3-Wheeled). FDA records list 131 510(k) clearances for Invacare Corp., from to . As of , FDA records show one recall naming K010135.

Clearance record

Decision date
Received
(30 days to decision)
Product code
INI Vehicle, Motorized 3-Wheeled
Regulation
21 CFR 890.3800
Device class
Class II
Review panel
Physical Medicine
Applicant
Invacare Corp. One Invacare Way, Elyria OH
510(k) summary
Summary
Third party review
No

Clearances, product code INI

Trailing 12 months
22 clearances under product code INI in the twelve months to October 2026, January 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code INI, trailing twelve months
MonthClearances
November 20251
December 20252
January 20265
February 20262
March 20262
April 20261
May 20261
June 20262
July 20262
August 20262
September 20262
October 20260