Bios S.R.L. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Bios S.R.L. has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Silver Spring, US.
Latest FDA clearance: Dec 2024. Active since 2005.
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 Bios S.R.L.
14 devices
Cleared
Dec 30, 2024
Splendor X (Alex, Alex2, Nd:YAG, Alex+Nd:YAG)
General & Plastic Surgery
54d
Cleared
Jun 14, 2024
Splendor X (Alex, Alex2, Nd:YAG, Alex+Nd:YAG)
General & Plastic Surgery
28d
Cleared
Oct 30, 2023
NuEra Tight RF Model OptiStream
General & Plastic Surgery
227d
Cleared
Aug 11, 2023
NuEra Tight RF Family
General & Plastic Surgery
231d
Cleared
May 02, 2023
NuEra Tight RF Model APMD145.M70-US
General & Plastic Surgery
125d
Cleared
Apr 21, 2021
NuEra Tight RF, NuEra Tight RF Plus
General & Plastic Surgery
29d
Cleared
Dec 31, 2020
NuEra Tight Family, EMS Model
Physical Medicine
238d
Cleared
Aug 11, 2020
NuEra Tight, NuEra Tight EMS
General & Plastic Surgery
180d
Cleared
Dec 08, 2016
FAMILY OF SQUARE EPIL (Alex, Alex2, Nd:Yag, Alex+Nd:Yag)
General & Plastic Surgery
178d
Cleared
Apr 12, 2016
Superbium
General & Plastic Surgery
158d
Cleared
Nov 19, 2015
Family of Radiofrequency System (Biorevital RF MED, ThermiSmooth 250)
General & Plastic Surgery
188d
Cleared
May 15, 2008
BIOSYAG MEDICAL SYSTEM
General & Plastic Surgery
93d