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

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MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526743670·ACHIMED ACHILLES SUPP SILVER IV

MEDIAL ROTATION KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDIAL ROTATION KNEE

FDA Adverse Event
Injury ·MATORTHO LIMITED·Product code JWH·January 22, 2016

MEDIAL ROATION KNEE

FDA Adverse Event
Malfunction ·MATORTHO LIMITED·Product code JWH·January 22, 2016

MEDIAL ROATION KNEE

FDA Adverse Event
Injury ·MATORHTO LIMITED·Product code JWH·January 22, 2016

MEDIAL ROTATION KNEE

FDA Adverse Event
Malfunction ·MATORTHO LIMITED·Product code JWH·January 22, 2016

MEDIAL ROTATION KNEE

FDA Adverse Event
Injury ·MATORTHO LIMITED·Product code JWH·January 22, 2016

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·H65820202141·Channels PT NiTi Rotary File

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526743557·LEVAMED ANKLE SUPPORT SILVER IV

OsteoMed

FDA UDI
OSTEOMED LLC·00845694000239·2.0mm x 14mm Locking Screw

APEX PS Knee

FDA UDI
Omni Life Science, Inc.·00841690113102·PS Insert, Size 2 x 14mm

neoWave LS

FDA UDI
XENIX MEDICAL LLC·00818345023970·PADDLE SPREADER, 14MM

InTess Lumbar Cage

FDA UDI
Kalitec Direct LLC·B07312K0102140·Shaver, Open 14mm

Specials

FDA UDI
Seaspine Orthopedics Corporation·10889981153526·Trial, 7x24, 14mm

SINUSCOPE AND BACCESSORIES

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

FIRSTSAVE BIPHASIC MODEL #9200 AND 9210

FDA 510(k)
FDA Class 3 ·Cardiovascular

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE SUZHOU·Product code ITI·March 25, 2013

HEARTMATE II LVAS

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·March 16, 2011

ACCU-CHEK ACTIVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 26, 2008

BATTERY,PAD-PAK-03

FDA Adverse Event
Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·August 17, 2020