11 results
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20ms
·
Sources: EU EUDAMED, US FDA
MONOPOLAR SUCTION CANNULA; MONOPOLAR ELECTRODES
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
RAPID Graft Delivery
FDA UDI
Seaspine Orthopedics Corporation·10889981140946·Graft Loading Block, Graft Delivery
SmartClaw Thrombectomy Catheter, 20 mm (FD0660-01), SmartClaw Thrombectomy Catheter, 32 mm (FD0660-02)
FDA 510(k)
FDA Class 2
·Cardiovascular
NOVABONE BIOACTIVE STRIP
FDA 510(k)
FDA Class 2
·Orthopedic
ZIPLOOP BUTTON 10MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBI·December 3, 2020
ZIPLOOP INLINE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HWC·January 12, 2021
RESTORE PRIME ADVANCED
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·December 22, 2010
12/14 ARTICUL 40MM M SPEC+5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code LPH·February 4, 2013
BI-METRIC/X POR NC 8X120
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·July 17, 2014
HEMOCHRON SIGNATURE ELITE
FDA Adverse Event
Malfunction
·ACCRIVA DIAGNOSTICS·Product code JPA·May 25, 2016
Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025