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
K893992Substantially Equivalent

Noetix, Biopsy Needle

Noetix, Inc., Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893992 is the FDA 510(k) clearance record for NOETIX, BIOPSY NEEDLE, a class II device, cleared for Noetix, Inc. on under FDA product code KNW (Instrument, Biopsy). FDA records list 3 510(k) clearances for Noetix, Inc., from to . As of , FDA records show no recalls naming K893992.

Clearance record

Decision date
Received
(95 days to decision)
Product code
KNW Instrument, Biopsy
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Noetix, Inc. 5602 Elmwood Ave., Suite 122,, Indianapolis IN
Third party review
No

Clearances, product code KNW

Trailing 12 months
8 clearances under product code KNW in the twelve months to October 2026, August 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code KNW, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20260
July 20260
August 20264
September 20260
October 20260