Bio-Med USA, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Bio-Med USA, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Paterson, US.
Last cleared in 2022. Active since 2008.
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 Bio-Med USA, Inc.
10 devices
Cleared
Aug 09, 2022
IRIS Pi Q switched Nd YAG laser
General & Plastic Surgery
49d
Cleared
Oct 06, 2021
Picore
General & Plastic Surgery
96d
Cleared
Nov 02, 2018
Cellene CO2 Laser System
General & Plastic Surgery
72d
Cleared
May 15, 2017
Dental 5 Multi Diode laser
General & Plastic Surgery
143d
Cleared
Sep 24, 2014
LUCID LY
General & Plastic Surgery
175d
Cleared
Jun 06, 2014
ATOVEN
General & Plastic Surgery
176d
Cleared
May 09, 2013
UNITOX BOTOX SYRINGE
General Hospital
156d
Cleared
Dec 20, 2012
WANDY DISPERSVIE ELECTRODE
General & Plastic Surgery
238d
Cleared
Dec 19, 2011
MX-7000 MICROXEL
General & Plastic Surgery
174d
Cleared
Sep 08, 2008
BIO-MED SOFT INSULIN SYRINGE: MODELS 1CC, 0.5CC, 0.3CC
General Hospital
98d