18 results · 23ms · Sources: EU EUDAMED, US FDA

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Sterile Dilator

FDA 510(k)
FDA Class 2 ·Cardiovascular

NA

FDA UDI
Stryker GmbH·07613154481958·Drill, WL 26.5mm, Stryker-Shaft

Sklar

FDA UDI
SKLAR CORPORATION·10649111452079·BROWN RESANO DRESS FORCEPS 8 INCHES

SP-FIX SPINOUS PROCESS FIXATION PLATE

FDA 510(k)
FDA Class 2 ·Orthopedic

CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

N/A

FDA UDI
Exactech, Inc.·10885862659897·Trial, Monobloc Revision Stem

NA

FDA UDI
Exactech, Inc.·10885862282811·TRIAL, MONOBLOC REVISION STEM, 19x195mm

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 23, 2023

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·June 13, 2018

FINELINE II

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code DTB·April 10, 2017

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011

ACCENT DR RF

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 20, 2013

UNKNOWN PROGRIP MESH PRODUCT

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION·Product code FTL·March 20, 2015

FLEXTEND

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVN·July 20, 2011

UNKNOWN PROGRIP MESH PRODUCT

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION·Product code FTL·March 11, 2015

ENDOPATH*MULTIFEED STAPLER

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·August 16, 2019

PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTL·August 22, 2019