510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K843816Substantially Equivalent

Tal-Clip

Talboy, Inc., Boise ID / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843816 is the FDA 510(k) clearance record for TAL-CLIP, a class I device, cleared for Talboy, Inc. on under FDA product code GDJ (Clamp, Surgical, General & Plastic Surgery). FDA records list one 510(k) clearance for Talboy, Inc. As of , FDA records show no recalls naming K843816.

Clearance record

Decision date
Received
(33 days to decision)
Product code
GDJ Clamp, Surgical, General & Plastic Surgery
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Talboy, Inc. P.O. Box 2831, Boise ID
Third party review
No

Clearances, product code GDJ

Trailing 12 months

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

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