FDA Device Intelligence
Home › SEIRIN CORPORATION › SEIRIN ACUPUNCTURE NEEDLE

SEIRIN ACUPUNCTURE NEEDLE

SEIRIN CORPORATION · Model KB-Type No.3(0.20)x150mm · UDI-DI 04547248240288

MQX Prescription
10
510(k) clearances
13
Adverse events
1
Recalls
72
Facilities

Description

Metal Handle with Guide Tube

Recalls

DateFirmReason
2007-11-28Marknew ProductsMarketed without 510(k)

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 docs
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.