510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770217Substantially Equivalent

Lance Ltd. Steri. Stitch Cutter Blade

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

K770217 is the FDA 510(k) clearance record for LANCE LTD. STERI. STITCH CUTTER BLADE, a class I device, cleared for Aeroceuticals on under FDA product code GES (Blade, Scalpel). FDA records list 5 510(k) clearances for Aeroceuticals, from to . As of , FDA records show no recalls naming K770217.

Clearance record

Decision date
Received
(56 days to decision)
Product code
GES Blade, Scalpel
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Aeroceuticals 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GES

Trailing 12 months

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

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