510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K800373Substantially Equivalent

Tenderlift

Competent Design, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K800373 is the FDA 510(k) clearance record for TENDERLIFT, a class I device, cleared for Competent Design on under FDA product code FMR (Device, Transfer, Patient, Manual). FDA records list one 510(k) clearance for Competent Design. As of , FDA records show no recalls naming K800373.

Clearance record

Decision date
Received
(21 days to decision)
Product code
FMR Device, Transfer, Patient, Manual
Regulation
21 CFR 880.6785
Device class
Class I
Review panel
General Hospital
Applicant
Competent Design 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FMR

Trailing 12 months

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

FDA records show no clearances under product code FMR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FMR, 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