Home › Device types › ION
Exerciser, Non-Measuring
FDA product code ION · Class 1 · Physical Medicine
444
Registered devices
117
Adverse events
2
Recalls
43
510(k) clearances
Devices with this code
Pedal Exerciser, Non-Folding, Hands/Feet — Dynarex CorporationM.A.S.S. Traction Belt — M.A.S.S. Rehab, LLCVector Base — Bioness Medical, Inc.ReJoyce — Rehabtronics IncSmall Tricycle — RIFTON EQUIPMENTValedo — HOCOMA AGMAT PLATFORM,4X7,NAT,BLUE — Hausmann Enterprises, LLCMAT PLATFORM,WALL 4x7,FOLK,BLUE,(2 PC) — Hausmann Enterprises, LLCOmniTour System — ACCELERATED CARE PLUS CORPMAT PLATFORM,HYDR,BLUE,6X8' — Hausmann Enterprises, LLCSTAIRS,ADA CONVERTIBLE,11" DEEP STEP — Hausmann Enterprises, LLCMAT PLTFRM,WALL,5X7,OAK,Black — Hausmann Enterprises, LLCMcKesson — MCKESSON MEDICAL-SURGICAL INC.DeRoyal — DEROYAL INDUSTRIES, INC.Tangle, Inc. — Tangle, Inc.SILVERSTAR. TWO SIDED STAIRCASE — Hausmann Enterprises, LLCBIKO — ORMESA SRLMcKesson — MCKESSON MEDICAL-SURGICAL INC.BIKO — ORMESA SRLT-FOAM CUBES VARIETY PACK 4 OF EACH COLOR — ALIMED, INC.OraStretch® Press Device – Pediatric — Cranio Mandibular Rehab, Inc.TABLE,HAND THERAPY,HYDR,48X32X27-39" — Hausmann Enterprises, LLCBIKO — ORMESA SRLPUTTY ALIMED THERAPY TAN CODED 5LBS — ALIMED, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-03-27 | Amtryke LLC | Product is being recalled due to complaints of cracked frames. |
| 2011-07-11 | North Coast Medical Inc | Potential for plastic D-ring to break during use and cause injury. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
