510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K943719Substantially Equivalent

Visistat Stapler

Pilling Weck, Inc., Research Triangle Park NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K943719 is the FDA 510(k) clearance record for VISISTAT STAPLER, a class I device, cleared for Pilling Weck, Inc. on under FDA product code GDT (Staple, Removable (Skin)). FDA records list 6 510(k) clearances for Pilling Weck, Inc., from to . As of , FDA records show no recalls naming K943719.

Clearance record

Decision date
Received
(23 days to decision)
Product code
GDT Staple, Removable (Skin)
Regulation
21 CFR 878.4760
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Pilling Weck, Inc. 1 Weck Dr., Research Triangle Park NC
510(k) summary
Statement
Third party review
No

Clearances, product code GDT

Trailing 12 months

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

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