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Astek

Young Innovations, Inc. · Model 23014ASTEK3KIT · UDI-DI 00840326421925

EJI
10
510(k) clearances
34
Adverse events
1
Recalls
78
Facilities

Description

inSafe Syringe, 2.2ml, O Ring Asp., Thumb Ring 3 Kit

Recalls

DateFirmReason
2015-02-11Milestone Scientific, Inc.Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.

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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.