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
K941161Substantially Equivalent

Flexible Grasping Forceps

Surgical Technologies, Inc., Miami Lakes FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K941161 is the FDA 510(k) clearance record for FLEXIBLE GRASPING FORCEPS, a class II device, cleared for Surgical Technologies, Inc. on under FDA product code EOQ (Bronchoscope (Flexible Or Rigid)). FDA's definition for product code EOQ reads: "A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. If the...". FDA records list 28 510(k) clearances for Surgical Technologies, Inc., from to . As of , FDA records show no recalls naming K941161.

Clearance record

Decision date
Received
(54 days to decision)
Product code
EOQ Bronchoscope (Flexible Or Rigid)
Regulation
21 CFR 874.4680
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Surgical Technologies, Inc. 4715 NW 157th St., Suite 212, Miami Lakes FL
510(k) summary
Summary
Third party review
No

Clearances, product code EOQ

Trailing 12 months
11 clearances under product code EOQ in the twelve months to October 2026, September 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code EOQ, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20260
March 20260
April 20262
May 20261
June 20261
July 20262
August 20260
September 20263
October 20260