17 results · 24ms · Sources: EU EUDAMED, US FDA

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PSA ANTIBODY KIT

FDA 510(k)
FDA Class 2 ·Immunology

Ophthalmic Spatula

FDA UDI
KATENA PRODUCTS, INC.·00841668115138·NAGAHARA/BECHERT MANIPULATOR DOUBLE-ENDED

BEHIND-THE-EAR #123 AGCI

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

IONSIL GEL

FDA 510(k)
FDA Unclassified ·Unknown

CONVERTBL I.V.DUAL CHANNEL HSP

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 20, 2011

CONVERTBL I.V..DUAL C

FDA Adverse Event
Malfunction ·HOSPIRA LTD.·Product code FPA·August 13, 2009

PRIMARY PLUMSET PP YSITE 272CM NDEHP

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·March 19, 2012

CONVERTBL I.V. DUAL C

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 15, 2009

CONVERTBL I.V. DUAL CHANNEL HSP

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·July 7, 2011

UNK

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 15, 2009

GREENLIGHT MOXY FIBER OPTIC

FDA Adverse Event
Malfunction ·AMERICAN MED SYS·Product code GEX·January 22, 2013

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·December 17, 2010

ENDO LINEAR CUTTERS - ETS45MM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 14, 2014

IMMULITE 2000 ESTRADIOL

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CHP·December 6, 2024

IMMULITE 2000 ESTRADIOL

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CHP·December 6, 2024

IMMULITE 2000 ESTRADIOL

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CHP·December 6, 2024

TI Single Vector Distractor Body with Right Foot/30mm; Catalog ID 487.964 The Titanium Single Vector Distractor and Proximal Foot Plates are intended for mandibular bone lengthening where gradual bone distraction is required, including conditions such as congenital mandibular deficiencies or post-traumatic defects.

FDA Enforcement
Class II ·Terminated·Synthes (USA) Products LLC·August 24, 2016