81 results
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20ms
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Sources: EU EUDAMED, US FDA
MODIFICATION TO DIADEXUS PLAC TEST
FDA 510(k)
FDA Class 2
·Immunology
Premier
FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·D6911040101·RING PESSARY-SUPPORT#1
Orthopedic manual surgical instrument
FDA UDI
BAUI BIOTECH CO. LTD.·04718005155484·Torque Wrench 3N-m
23GA Illuminating Laser Probe, SMA906
FDA UDI
Peregrine Surgical, Llc·00632307001970·23GA Illuminating Laser Probe, SMA906
LOCATOR F-Tx
FDA UDI
Zest Anchors, LLC·00840481115202·F-Tx Attachment System, Regular CrossFit (RC) C...
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481110399·LOCATOR Abutment R-Tx, Regular CrossFit Interna...
Cytoflex Textured Tef-Guard
FDA UDI
UNICARE BIOMEDICAL INC.·D767C0401010·Cytoflex® Tef-Guard® is a non-resorbable membra...
RX VIATRAC 14 PERIPHERAL DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PROMUS PREMIER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·December 20, 2024
LEAD MODEL 303
FDA Adverse Event
Malfunction
·LIVANOVA USA, INC.·Product code LYJ·May 27, 2021
BD BACTEC¿ MGIT¿ 960 PZA MEDIUM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MJA·October 20, 2023
SPRINT QUATTRO SECURE S MRI SURESCAN
FDA Adverse Event
Injury
·MPRI·Product code LWS·February 6, 2024
CRE PRO
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·February 23, 2026
LUGE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·April 3, 2024
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 8, 2022
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·April 3, 2013
ARTICULEZE M 28MM 1.5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD·Product code LPH·May 7, 2008
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 5, 2011
LEAD MODEL 304
FDA Adverse Event
Malfunction
·LIVANOVA USA, INC.·Product code LYJ·July 15, 2021