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

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Disposable Surgical Mask

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

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113356·CLEAR CORNEA KNIFE 2.8MM (BX/5)

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113363·CLEAR CORNEA KNIFE 3.0MM (BX/5)

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113288·STAB KNIFE 22.5 DEGREE (BX/5)

NOBELACTIVE TIULTRA NP 3.5X13MM

FDA Adverse Event
Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

NOBELACTIVE TIULTRA NP 3.5X13MM

FDA Adverse Event
Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102457·MAXTM HXL Patella Component Sz 3 34mm 9.0mm Thick

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102464·MAXTM HXL Patella Component Sz 4 38mm 9.5mm Thick

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150793·Patella Instrument Case

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102440·MAXTM HXL Patella Component Sz 2 30mm 8.5mm Thick

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102471·MAXTM HXL Patella Component Sz 5 42mm 10.0mm Thick

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102433·MAXTM HXL Patella Component Sz 1 27mm 8.0mm Thick

TERABYTE 2000 HAIR REMOVER

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

THERMAL CAUTERY UNIT, MODEL 150

FDA 510(k)
FDA Class 2 ·Ophthalmic

EKOSONIC KIT 106CM 12CM TZ

FDA Adverse Event
Death ·BOSTON SCIENTIFIC CORPORATION·Product code KRA·November 16, 2023

BECKMAN-COULTER ANALYZER

FDA Adverse Event
Injury ·BECKMAN-COULTER·Product code GKZ·October 15, 2008

PARIETEX UGYTEX PP 15X10CM X1

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION·Product code FTL·June 21, 2013

SPACEMAKER PREPERITONEAL DIST BALLOON

FDA Adverse Event
Injury ·USSC PUERTO RICO·Product code GCJ·August 3, 2011

PULSE

FDA Adverse Event
Injury ·LUMENIS LTD·Product code GEX·August 22, 2024

VERSAPULSE POWERSUITE

FDA Adverse Event
Injury ·LUMENIS LTD·Product code GEX·August 19, 2024