Atlas FDA

Bioness, Inc.

13 FDA 510(k) clearances · Manufacturer

Sort:Newest firstOldest first

Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free

RecordFirmDate
StimRouter Neuromodulation System (K211965)Bioness, Inc.2022-02-23
StimRouter Neuromodulation System (K200482)Bioness, Inc.2020-03-27
L100 Go System (K200262)Bioness, Inc.2020-03-04
StimRouter Neuromodulation System (K190047)Bioness, Inc.2019-10-31
L360 Thigh System (K191587)Bioness, Inc.2019-09-12
L300 Go System (K190285)Bioness, Inc.2019-03-14
L300 Go System (K173682)Bioness, Inc.2018-03-09
L300 Go System (K162407)Bioness, Inc.2017-01-27
StimRouter Lead Kit/StimRouter Surgical Tool Kit/StimRouter Clinician Kit/StimRouter User Kit (K142432)Bioness, Inc.2015-02-20
H200 WIRELESS HAND REHABILITATION SYSTEM WITH OPTIONAL INTELLI-CONNECT EARPIECE TRIGGERING DEVICE (K123636)Bioness, Inc.2013-05-01
NESS L300 SYSTEM KIT, LEF MODEL LG3-5100; NESS L300 SYSTEM KIT, RIGHT MODEL LG3-5000; SMALL NESS L300 SYSTEM KIT, RIGHT (K122784)Bioness, Inc.2012-12-27
NESS L300 SYSTEM KIT, LEFT, NESS L300 SYSTEM KIT, RIGHT, SMALL NESS L300 SYSTEM KIT, RIGHT, SMALL NESS L300 SYSTEM KIT, (K120853)Bioness, Inc.2012-04-20
L300 PLUS SYSTEM (RIGHT, LEFT), L300 PLUS SYSTEM UPGRADE KIT (RIGHT, LEFT) (K103343)Bioness, Inc.2011-04-29

Track Bioness, Inc. automatically

Every clearance here is in the API, with alerts when new ones post.