21 results · 29ms · Sources: EU EUDAMED, US FDA

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KATANA AVENCIA Block

FDA 510(k)
FDA Class 2 ·Dental

BBIG

FDA UDI
BBig B.V.·08719616026183·M153476

BINAXNOW COVID-19 ANTIGEN SELF TEST OTC 2 TEST PACK

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QKP·June 18, 2021

BINAX NOW COVID-19 HOME TEST

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 5, 2021

BINAXNOW¿ COVID-19 ANTIGEN SELF TEST

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 11, 2021

BINAXNOW COVID-19 AG SELF TEST

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QKP·July 23, 2021

BRIVOXR285AMX, OPTIMA XR200AMX, OPTIMAXR220AMX

FDA 510(k)
FDA Class 2 ·Radiology

ALLWOUND

FDA 510(k)
FDA Unclassified ·Unknown

BINAXNOW¿ COVID-19 ANTIGEN SELF TEST OTC

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QKP·May 31, 2021

BINAXNOW¿ COVID-19 ANTIGEN SELF TEST

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·July 30, 2021

BINAXNOW¿ COVID-19 ANTIGEN SELF TEST

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·July 30, 2021

BINAXNOW¿ COVID-19 ANTIGEN SELF TEST

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·July 30, 2021

BINAX NOW COVID-19 AG CARD

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 18, 2021

BINAXNOW¿ COVID-19 ANTIGEN SELF TEST

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QKP·June 25, 2021

ELLIPSE DR

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·October 8, 2014

N/A

FDA Adverse Event
Injury ·IPG MFG SWITZERLAND·Product code NIK·June 8, 2013

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM

FDA Adverse Event
Malfunction ·ALLERGAN·Product code LTI·June 21, 2011

BINAXNOW¿ COVID-19 ANTIGEN SELF TEST

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 19, 2021

1.55MM X 10MM FLUTED TWIST DRL

FDA Adverse Event
Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBE·October 17, 2016

1.55MM X 10MM FLUTED TWIST DRL

FDA Adverse Event
Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBE·October 17, 2016