64 results
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24ms
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Sources: EU EUDAMED, US FDA
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Country: United States
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VitalBeam
FDA 510(k)
FDA Class 2
·Radiology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694018999·2.0mm X 13mm Cannulated Headless Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694068420·Cannulated 2.0 x 13mm Headless Screw Sterile Qty 5
SANTORINI Corpectomy Cage System
FDA UDI
VB Spine LLC·10888857243132·Bone Packing Mold Size 12x14 mm
EVOLVE(R) HPD 980/1470NM MULTIWAVELENGTH DIODE LASER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ENDEAVOR RESOLUTE RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·September 22, 2016
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 30, 2012
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL·Product code NAY·June 3, 2013
ALARIS
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·July 13, 2011
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·September 18, 2008
ONYX
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 16, 2023
Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to facilitate the implantation of joint replacement implants.
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·June 15, 2016
SoftPath Laboratory Information System. Versions 4.3.0.8, 4.3.0.9, 4.3.0.10, 4.3.0.11, 4.3.0.12, 4.3.0.14, 4.3.0.15, and 4.4.0.0
FDA Enforcement
Class II
·Terminated·SCC Soft Computer·February 18, 2015
Microscan Synergies Plus Negative Urine Combo 2 Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for gram-negative bacteria.
FDA Enforcement
Class I
·Terminated·Siemens Healthcare Diagnostics, Inc.·September 18, 2013
Minor Ortho Pack, Kit number 002646-12 and 002646-13 convenience custom kits used for general surgery in hospital operating room
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·October 26, 2016
Major Ortho Pack, kit number 002647-12 and 002647-13 convenience custom kits used for general surgery in hospital operating room
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·October 26, 2016
ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process.
FDA Recall
Terminated
·Trumpf Medical Systems·Product code JEA·July 24, 2013
LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848; 14060546846; 14060546845; 14060546933; 14060546932; 14060546852; 14060546850; 14060546847. The intended use of this device is for storage of specimens/tissues during processing.
FDA Recall
Terminated
·Leica Microsystems, Inc.·Product code IDZ·April 4, 2013
The Constellation Vision System Pneumatic Handpiece. Indicated for both anterior and posterior segment opthalmic surgery.
FDA Recall
Terminated
·Alcon Grieshaber AG Winkelriedstrasse 52 Schaffhausen Switzerland·Product code HQE·April 17, 2013
FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray.
FDA Recall
Terminated
·American Optisurgical Inc·Product code OJU·April 30, 2013