50 results · 22ms · Sources: EU EUDAMED, US FDA

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Electronic Blood Pressure Monitor

FDA 510(k)
FDA Class 2 ·Cardiovascular

OPERATING SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896055520·OPERATING SCISSORS STRAIGHT SHARP BLADES POWER ...

RETRACTOR CHEEK/LIP, 10 x 40MM TOE UP

FDA UDI
W.H. Holden, Inc.·D9282007160·

RETRACTOR CHEEK/LIP, 10 x 55MM TOE UP

FDA UDI
W.H. Holden, Inc.·D92820071610·

RETRACTOR CHEEK/LIP, 10 x 65MM TOE UP

FDA UDI
W.H. Holden, Inc.·D9282007161SPEC0·

RETRACTOR CHEEK/LIP, 10 x 80MM TOE UP

FDA UDI
W.H. Holden, Inc.·D92820071620·

Orbitum Staple System

FDA UDI
CPM Medical Consultants, LLC·B565FO2007161·Punch VI 16mm

RAPID OPIATES TEST STRIP II, RAPID OPIATES TEST CARD II AND DOA MULTIPLE DRUG TEST CARDS (UP TO SIX TESTS)

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

ACCESS CK-MB ON THE ACCESS IMMUNOASSAY ANALYZER

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

CADD CASSETTE 100ML W/FLOWSTOP

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·March 2, 2022

PULSE GEN MODEL UNK

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·February 29, 2008

PULSE GEM MODEL UNK

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·February 29, 2008

PULSE GEN MODEL UNK

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·February 29, 2008

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

GORE PRECLUDE DURA SUBSTITUTE

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code GXQ·June 25, 2013

GORE PRECLUDE DURA SUBSTITUTE

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code GXQ·June 25, 2013

GORE PRECLUDE DURA SUBSTITUTE

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code GXQ·June 26, 2013

GORE PRECLUDE DURA SUBSTITUTE

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code GXQ·June 26, 2013

GORE PRECLUDE DURA SUBSTITUTE

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code GXQ·June 25, 2013

DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM DEXCOM SHARE SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·October 29, 2015