510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771187Substantially Equivalent

Dermahook #382-805

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

K771187 is the FDA 510(k) clearance record for DERMAHOOK #382-805, a class I device, cleared for Edward Weck, Inc. on under FDA product code GDG (Hook, Surgical, General & Plastic Surgery). FDA records list 140 510(k) clearances for Edward Weck, Inc., from to . As of , FDA records show 2 recalls naming K771187.

Clearance record

Decision date
Received
(10 days to decision)
Product code
GDG Hook, Surgical, General & Plastic Surgery
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Edward Weck, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GDG

Trailing 12 months

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

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