510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023450Substantially Equivalent

Biopsy Site Tissue Marker Device

Promex, Inc., Franklin IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K023450 is the FDA 510(k) clearance record for BIOPSY SITE TISSUE MARKER DEVICE, a class II device, cleared for Promex, Inc. on under FDA product code NEU (Marker, Radiographic, Implantable). FDA records list 18 510(k) clearances for Promex, Inc., from to . As of , FDA records show no recalls naming K023450.

Clearance record

Decision date
Received
(65 days to decision)
Product code
NEU Marker, Radiographic, Implantable
Regulation
21 CFR 878.4300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Promex, Inc. 3049 Hudson St., Franklin IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NEU

Trailing 12 months
4 clearances under product code NEU in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code NEU, trailing twelve months
MonthClearances
November 20250
December 20253
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260