510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902141Substantially Equivalent

Anolift - Portable & Anolift - Gantry

Anodyne, Brighton MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902141 is the FDA 510(k) clearance record for ANOLIFT - PORTABLE & ANOLIFT - GANTRY, a class I device, cleared for Anodyne Corp. on under FDA product code FSA (Lift, Patient, Non-Ac-Powered). FDA records list 2 510(k) clearances for Anodyne Corp., from to . As of , FDA records show no recalls naming K902141.

Clearance record

Decision date
Received
(120 days to decision)
Product code
FSA Lift, Patient, Non-Ac-Powered
Regulation
21 CFR 880.5510
Device class
Class I
Review panel
General Hospital
Applicant
Anodyne Corp. 4023 S. U.S. 23, Suite #106, Brighton MI
Third party review
No

Clearances, product code FSA

Trailing 12 months

FDA records hold no clearances under product code FSA in the trailing twelve months.

FDA records show no clearances under product code FSA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FSA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260