510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932534Substantially Equivalent

Isi Fenestrated Dissecting and Grasping Forceps

Innovative Surgical, Inc., West Palm Beach FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932534 is the FDA 510(k) clearance record for ISI FENESTRATED DISSECTING AND GRASPING FORCEPS, a class I device, cleared for Innovative Surgical, Inc. on under FDA product code GFI (Osteotome, Manual). FDA records list 7 510(k) clearances for Innovative Surgical, Inc., from to . As of , FDA records show no recalls naming K932534.

Clearance record

Decision date
Received
(83 days to decision)
Product code
GFI Osteotome, Manual
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Innovative Surgical, Inc. 3071 Continental Dr.,, West Palm Beach FL
510(k) summary
Statement
Third party review
No

Clearances, product code GFI

Trailing 12 months

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

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