510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K852567Substantially Equivalent

3M Fukuda Type Ring Retractor

3M Company, Cottae Grove MN / Traditional, Substantially Equivalent

K852567 is the FDA 510(k) clearance record for 3M FUKUDA TYPE RING RETRACTOR, a class I device, cleared for 3M Company on under FDA product code GAD (Retractor). FDA records list 63 510(k) clearances for 3M Company, from to . As of , FDA records show no recalls naming K852567.

Clearance record

Decision date
Received
(21 days to decision)
Product code
GAD Retractor
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
3M Company Chemolite Blvd. & Washington, Cottae Grove MN
Third party review
No

Clearances, product code GAD

Trailing 12 months

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

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