14 results · 20ms · Sources: EU EUDAMED, US FDA

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DAVID PREGNANCY TEST (MIDSTREAM)

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Premier K-FILES

FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·D6919053236·FILES PKG 6 25MM 30

LUXABITE

FDA 510(k)
FDA Class 2 ·Dental

RETINADX

FDA 510(k)
FDA Class 2 ·Ophthalmic

METASUL DUROM, COMPONENT FOR ACETABULUM, UNCEMENTED, 48, 42,CODE H

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·June 19, 2018

VITALITY 2

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 11, 2013

ADAPTA SR

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·April 13, 2011

FOOTED ATTACHMENT 2.4MM LEGEND, AF02 (B-1)

FDA Adverse Event
Malfunction ·MEDTRONIC POWERED SURGICAL SOLUTIONS·Product code HBB·May 28, 2008

METASUL DUROM, COMPONENT FOR ACETABULUM, UNCEMENTED, 54, 48, CODE N

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·March 28, 2019

METASUL DUROM, COMPONENT FOR ACETABULUM, UNCEMENTED, 50, 44, CODE J

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·February 20, 2018

METASUL DUROM, COMPONENT FOR ACETABULUM, UNCEMENTED, 50, 44, CODE J

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·February 20, 2018

METASUL DUROM, COMPONENT FOR ACETABULUM, UNCEMENTED, 46/ 40, CODE F

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·June 13, 2018

METASUL DUROM, COMPONENT FOR ACETABULUM, UNCEMENTED, 62/56, CODE V

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·January 31, 2018

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012