510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K861806Substantially Equivalent

Medcare Suture Scissors (Suture/gauze Weight)

Medcomp Technologies, Inc., Penfield NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K861806 is the FDA 510(k) clearance record for MEDCARE SUTURE SCISSORS (SUTURE/GAUZE WEIGHT), a class II device, cleared for Medcomp Technologies, Inc. on under FDA product code KDA (Prosthesis, Ptfe/Carbon-Fiber). FDA records list 5 510(k) clearances for Medcomp Technologies, Inc., from to . As of , FDA records show no recalls naming K861806.

Clearance record

Decision date
Received
(14 days to decision)
Product code
KDA Prosthesis, Ptfe/Carbon-Fiber
Regulation
21 CFR 878.3500
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medcomp Technologies, Inc. 2555 Baird Rd., Penfield NY
Third party review
No

Clearances, product code KDA

Trailing 12 months

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

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