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Activator Methods

Activator Methods International, Ltd. · Model ARIV Dark Blue · UDI-DI 00850021303136

LXM
1
510(k) clearances
8
Adverse events
1
Recalls
13
Facilities

Description

Chiropractic Adjusting Instrument

Recalls

DateFirmReason
2013-03-06Advanced Orthogonal Equipment, IncorporatedUnapproved medical device

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.