Home › SEIRIN CORPORATION › SEIRIN PYONEX NEEDLES

SEIRIN PYONEX NEEDLES

SEIRIN CORPORATION · Model Pyonex 0.20x1.7mm · UDI-DI 04547248420109

MQX Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Designed with both the patient and practitioner in mind, the new and advanced Pyonex™ Singles continue SEIRIN's tradition of gentle, painless and stress free press needles. The patented plastic case and sheath allow the practitioner to insert the needle without touching the needle tip or the surface of the Micropore adhesive tape. This hypoallergenic latex-free adhesive allows the skin to breathe during treatment. With SEIRIN's consistently smooth insertion, the result is a pleasant and painless experience for your patient.

Recalls

Date	Firm	Reason
2007-11-28	Marknew Products	Marketed 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 key Read 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.