510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K862729Substantially Equivalent

Penn 3-Ring Handle

Penn Medical Devices, Inc., Basking Ridge NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862729 is the FDA 510(k) clearance record for PENN 3-RING HANDLE, a class II device, cleared for Penn Medical Devices, Inc. on under FDA product code FFL (Dislodger, Stone, Basket, Ureteral, Metal). FDA records list 8 510(k) clearances for Penn Medical Devices, Inc., from to . As of , FDA records show no recalls naming K862729.

Clearance record

Decision date
Received
(98 days to decision)
Product code
FFL Dislodger, Stone, Basket, Ureteral, Metal
Regulation
21 CFR 876.4680
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Penn Medical Devices, Inc. 12 Ridge St., Basking Ridge NJ
Third party review
No

Clearances, product code FFL

Trailing 12 months

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

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