Bioness, Inc.
Bioness, Inc. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2022.
Top product codes for Bioness, Inc.
Recent clearances by Bioness, Inc.
- K211965 — StimRouter Neuromodulation System
- K200482 — StimRouter Neuromodulation System
- K200262 — L100 Go System
- K190047 — StimRouter Neuromodulation System
- K191587 — L360 Thigh System
- K190285 — L300 Go System
- K173682 — L300 Go System
- K162407 — L300 Go System
- K142432 — StimRouter Lead Kit/StimRouter Surgical Tool Kit/StimRouter Clinician Kit/StimRouter User Kit
- K123636 — H200 WIRELESS HAND REHABILITATION SYSTEM WITH OPTIONAL INTELLI-CONNECT EARPIECE TRIGGERING DEVICE
- K122784 — NESS L300 SYSTEM KIT, LEF MODEL LG3-5100; NESS L300 SYSTEM KIT, RIGHT MODEL LG3-5000; SMALL NESS L300 SYSTEM KIT, RIGHT
- K120853 — NESS L300 SYSTEM KIT, LEFT, NESS L300 SYSTEM KIT, RIGHT, SMALL NESS L300 SYSTEM KIT, RIGHT, SMALL NESS L300 SYSTEM KIT,
- K103343 — L300 PLUS SYSTEM (RIGHT, LEFT), L300 PLUS SYSTEM UPGRADE KIT (RIGHT, LEFT)
Data sourced from openFDA. This site is unofficial and independent of the FDA.