Devicor Medical Products, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Devicor Medical Products, Inc. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Cincinnati, US.
Latest FDA clearance: Mar 2026. Active since 2012.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Devicor Medical Products, Inc.
16 devices
Cleared
Mar 04, 2026
Mammotome Prima™ MR Dual Vacuum-Assisted Breast Biopsy System Control Module
General & Plastic Surgery
28d
Cleared
Jan 23, 2026
HydroMARK™ Plus Breast Biopsy Site Marker (Dragonfly Shape)
General & Plastic Surgery
59d
Cleared
Oct 29, 2024
Mammotome AutoCore™ Single Insertion Core Biopsy System
General & Plastic Surgery
29d
Cleared
Jul 10, 2024
HydroMARK™ Plus Breast Biopsy Site Marker (Hummingbird Shape) (4010-02-15-T6)
General & Plastic Surgery
138d
Cleared
Jan 12, 2024
LumiMARK™ Biopsy Site Marker (LM0215T (Tulip Shape))
General & Plastic Surgery
137d
Cleared
Jul 13, 2023
HydroMARK Plus Breast Biopsy Site Marker
General & Plastic Surgery
373d
Cleared
Apr 21, 2022
HydroMARK Breast Biopsy Site Marker
General & Plastic Surgery
283d
Cleared
Apr 14, 2021
HydroMARK Breast Biopsy Site Marker
General & Plastic Surgery
30d
Cleared
Dec 16, 2020
HydroMARK Breast Biopsy Site Markers
General & Plastic Surgery
63d
Cleared
Aug 18, 2020
Mammotome Revolve Dual Vacuum Assisted Biopsy (VAB) System
General & Plastic Surgery
28d
Cleared
Jun 15, 2017
HydroMARK Breast Biopsy Site Markers
General & Plastic Surgery
90d
Cleared
Aug 08, 2016
Mammotome elite Biopsy System-13G Probe, Mammotome elite Biopsy System-10G...
Gastroenterology & Urology
229d