30 results · 38ms · Sources: EU EUDAMED, US FDA

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MOTO PFJ System

FDA 510(k)
FDA Class 2 ·Orthopedic

MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S5 RM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·March 8, 2024

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780165279·Integra® Jarit® Parker Retractor, 7", Double-En...

The Inseminator

FDA UDI
Coopersurgical, Inc.·00888937011494·Intrauterine Inseminator, 3.5 French, 4.5" Long...

Ophthalmic Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668113899·VISCO INJECTION CANNULA 26GA

Sonoma™

FDA UDI
Seaspine Orthopedics Corporation·10889981050764·Sonoma Anterior Cervical Plate 1 Level Plate, 22mm

Initia Total Hip System

FDA UDI
KYOCERA MEDICAL CORPORATION·04580810057914·"MXHO LINER 28-60/64 Size:28-60/62/64 Type:Elev...

Initia Total Hip System

FDA UDI
KYOCERA CORPORATION·04547898307744·MXHO LINER 28-60/64

PHOENIX SFS

FDA UDI
Orthofix US LLC·18257200009145·GUIDE WIRE, NITINOL, 19.5", SHARP

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306804939·Sheehan Osteotome, 2mm, 16cm

Manta Ray™

FDA UDI
Seaspine Orthopedics Corporation·10889981057015·Plate - 1 Level - 22 mm

NA

FDA UDI
aap Implantate AG·04042409079948·Cortical Screw 2.0, L 22

COLLAGRAFT STRIP BONE GRAFT MATRIX (FOR USE AS A BONE FILLER), MODEL 1X,3X,6X (1,3 OR 6 STRIPS PER BOX)

FDA 510(k)
FDA Class 2 ·Orthopedic

MB 102 MILLENNIUM BLADES

FDA 510(k)
FDA Class 1 ·Ophthalmic

COMPRESSURE FRACTURE REPAIR IMPLANT

FDA Adverse Event
Injury ·USI ORTHOPAEDICS LLC DBA U.S. ORTHOPAEDICS·Product code HTN·April 6, 2011

NA

FDA UDI
aap Implantate AG·04042409079955·Cortical Screw 2.0, L 22

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962160190·PICCOLO AUTOCLAVABLE PLASTIC TRAY, 9"X6"X2", LO...

ARCHITECT I1000SR

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·December 19, 2022

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·August 10, 2011

ACCU-CHEK COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 15, 2008