Bios S.R.L.
Bios S.R.L. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2024, with 1 FDA device recall on record.
Top product codes for Bios S.R.L.
FDA recalls by Bios S.R.L.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Bios S.R.L.
- K243445 — Splendor X (Alex, Alex2, Nd:YAG, Alex+Nd:YAG)
- K241407 — Splendor X (Alex, Alex2, Nd:YAG, Alex+Nd:YAG)
- K230755 — NuEra Tight RF Model OptiStream
- K223856 — NuEra Tight RF Family
- K223907 — NuEra Tight RF Model APMD145.M70-US
- K210867 — NuEra Tight RF, NuEra Tight RF Plus
- K201239 — NuEra Tight Family, EMS Model
- K200359 — NuEra Tight, NuEra Tight EMS
- K161632 — FAMILY OF SQUARE EPIL (Alex, Alex2, Nd:Yag, Alex+Nd:Yag)
- K153229 — Superbium
- K151296 — Family of Radiofrequency System (Biorevital RF MED, ThermiSmooth 250)
- K080374 — BIOSYAG MEDICAL SYSTEM
- K072344 — APL MEDICAL SYSTEM
- K043521 — BIOSYAG 50 MED
Data sourced from openFDA. This site is unofficial and independent of the FDA.