83 results · 25ms · Sources: EU EUDAMED, US FDA

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PARCUS 35 KNOTLESS PEEK CF PUSH-IN SUTURE ANCHORS, PARCUS 45 KNOTLESS PEEK CF PUSH-IN SUTURE ANCHORS

FDA 510(k)
FDA Class 2 ·Orthopedic

BIO-MODULAR SHOULDER SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304213449·

Bio-Modular® Shoulder System

FDA UDI
Biomet Orthopedics, LLC·00887868253546·

Marienfeld Superior

FDA UDI
Paul Marienfeld GmbH & Co. KG·04250317382719·

N/A

FDA UDI
HANS RUDOLPH, INC.·00874750004836·LARG QUEST MASK/HG GRN22OD SWL

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776164898·VEIN RETRACTOR BLADE

BIO-MODULAR SHOULDER SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304433687·

ARIEL RADIO FREQUENCY (RF) ELECTROSURGICAL CONTROL MODULE AND ACCESSORIES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

GE LUNAR VISCERAL FAT SOFTWARE

FDA 510(k)
FDA Class 2 ·Radiology

ARCHITECT SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·April 8, 2026

ARCHITECT SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·May 1, 2026

ALINITY I SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·May 4, 2026

ALINITY I SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·May 22, 2026

ZEPHIR

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·May 15, 2013

HEARTSTREAM FR2

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 17, 2014

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·June 2, 2011

ALINITY I SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·April 13, 2026

ALINITY I SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·May 18, 2026

ARCHITECT SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·April 22, 2026

ARCHITECT SYPHILIS TP REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LIP·May 19, 2026