510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925392Substantially Equivalent

Biopsy Forceps

Endo-Therapeutics, Inc., Safety Harbor FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925392 is the FDA 510(k) clearance record for BIOPSY FORCEPS, a class I device, cleared for Endo-Therapeutics, Inc. on under FDA product code FCL (Forceps, Biopsy, Non-Electric). FDA records list 7 510(k) clearances for Endo-Therapeutics, Inc., from to . As of , FDA records show no recalls naming K925392.

Clearance record

Decision date
Received
(375 days to decision)
Product code
FCL Forceps, Biopsy, Non-Electric
Regulation
21 CFR 876.1075
Device class
Class I
Review panel
Gastroenterology, Urology
Applicant
Endo-Therapeutics, Inc. 604-C Packard Ct., Safety Harbor FL
510(k) summary
Statement
Third party review
No

Clearances, product code FCL

Trailing 12 months

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

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