102 results
·
18ms
·
Sources: EU EUDAMED, US FDA
I TESTOTERONE
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ReLine
FDA UDI
Nuvasive, Inc.·00887517010469·RELINE-C Guide, Tap
Trumpf Medical
FDA UDI
Baxter Medical Systems GmbH + Co. KG·00887761996205·Hospital Device
Trimline
FDA UDI
ORMCO CORPORATION·00889989050790·UPPER RIGHT FIRST MOLAR TRIMLINE BAND SIZE 7
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690127642·AK3 Femoral Starter Drill
JUMAO OXYGEN CONCENTRATOR, MODEL JM-07000HI, JM-07000I, JM-07000
FDA 510(k)
FDA Class 2
·Anesthesiology
Vydence Laser Family
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197536097·Markham-Meyerding Laminectomy Retractor
24x65m...
N/A
FDA UDI
Zimmer GmbH·00889024277014·
NA
FDA UDI
Zimmer, Inc.·00889024152229·
Viant Medical, LLC
FDA UDI
VIANT MEDICAL·00840096403992·Adjustable Drill Guide
Continuum® Trilogy® Allofit® Longevity®
FDA UDI
Zimmer, Inc.·00889024152243·
Continuum® Trilogy® Allofit® Longevity®
FDA UDI
Zimmer, Inc.·00889024152250·
NA
FDA UDI
Zimmer, Inc.·00889024152205·
Continuum® Trilogy® Allofit® Longevity®
FDA UDI
Zimmer, Inc.·00889024152236·
NA
FDA UDI
Zimmer, Inc.·00889024152212·
NA
FDA UDI
Zimmer, Inc.·00889024152182·
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·HANCOCK MODIFIED ORIFICE BIOPROSTHESIS
MEGA NEEDLE DRIVER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·May 5, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012