15 results · 21ms · Sources: EU EUDAMED, US FDA

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QUIKCLOT HEMOSTATIC DRESSING

FDA 510(k)
FDA Unclassified ·Unknown

ArgenZ ST 98x18 ML OM1

FDA UDI
ARGEN CORPORATION, THE·D818123387·Dental porcelain/ceramic restoration kit

MISSION LIQUID URINE CONTROL, MISSION LIQUID DIPTUBE URINE CONTROL, MISSION DRY STRIP URINE CONTROL

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

CITIEFFE TITANIUM NAILING SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

LOGIC FEMORAL PS POR RIGHT SZ 2

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·February 10, 2025

PATIENT INFORMATION CENTER IX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·May 1, 2024

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

JAGWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code EZB·June 14, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

LOGIC CR FEMORAL POR, LEFT, SZ 3.5

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·December 11, 2024

LOGIC CR FEMORAL POR, RIGHT, SZ 3

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·May 14, 2019

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 26, 2023

PATIENT INFORMATION CENTER IX

FDA Adverse Event
Death ·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 9, 2023

Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model Numbers: GIF-1TH190, GIF-1TQ160, GIF-2T160, GIF-2TH180, GIF-H170, GIF-H180, GIF-H180J, GIF-H190, GIF-HQ190, GIF-LV1, GIF-N180, GIF-Q150, GIF-Q160Z, GIF-Q180, GIF-XP180N, GIF-XP190N, GIF-XTQ160. 510(k) Numbers: K112680, K954451, K051645, K100584, K111756, K011151, K123317.

FDA Enforcement
Class II ·Ongoing·Aizu Olympus Co., Ltd.·November 29, 2023

Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model Numbers: GIF-1TH190, GIF-1TQ160, GIF-2T160, GIF-2TH180, GIF-H170, GIF-H180, GIF-H180J, GIF-H190, GIF-HQ190, GIF-LV1, GIF-N180, GIF-Q150, GIF-Q160Z, GIF-Q180, GIF-XP180N, GIF-XP190N, GIF-XTQ160. 510(k) Numbers: K112680, K954451, K051645, K100584, K111756, K011151, K123317.

FDA Recall
Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·September 25, 2023