FDA Device Intelligence
HomeAnmuth Medical International, LLC › Anmuth Medical International

Anmuth Medical International

Anmuth Medical International, LLC · Model 72-181-16 · UDI-DI 08403207009340

FZZ
10
510(k) clearances
185
Adverse events
2
Recalls
183
Facilities

Description

Pitanguy Flap Demarcator small, 5.0 mm wide, 6-1/4" (15.9 cm)

Recalls

DateFirmReason
2013-07-10Precision Dynamics CorporationPDC Healthcare initiated this recall of Non-Sterile Viscot Part Number 1437-100 Surgical Skin Markers, becuase they were inadvertently mislabeled as PN STER-VIS Sterile Skin Marker
2012-08-22Viscot Medical LLCDual Tip Marker has inconsistent ink flow on the black permanent ink side.

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.