IROClass I

Vibrator, Therapeutic

Physical Medicine · 21 CFR 890.5975

MDR events5All time

Recalls2All time

Registered firms68Currently listed

510(k) clearances65All time

Recent MDR events

5 adverse event reports on file

Event type breakdown

Malfunction2

Unspecified1

Injury1

Other1

Most-reported manufacturers

*1 Connie Stevens Forever Spring Beauty System1 General Physiotherapy, Inc.1 Skinrecharge Llc1 Sunrise Medical Mpd1

Recalls

2 recall events for this product code

Non-Invasive Monitoring Systems, Inc.
TerminatedJun 18, 2012
US-001 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operation
Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling promotional materials which contain unsubstantiated direct and indirect claims.
Z-1819-2012 · View FDA record ↗
Non-Invasive Monitoring Systems, Inc.
TerminatedJun 18, 2012
USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operatio
Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling promotional materials which contain unsubstantiated direct and indirect claims.
Z-1820-2012 · View FDA record ↗

Registered firms

68 firms currently registered for this product code

510(k) clearances

65 clearances for this product code