134 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since launch in 2003); Multiple ImmunoCAP assays for Allergen Testing, FDA Cleared for use on Phadia 1000 instrument with IU statement-see attachments. Software utilized in multiple ImmunoCAP assays for Allergen Testing, FDA Cleared for use on Phadia 1000 instrument with IU statement-see attachments.
FDA Enforcement
Class II
·Terminated·Phadia US Inc·January 21, 2015
Merlin PCS 3650 Software Upgrade Kit, REF 3330 St. Jude Medical The MerlinTM Patient Care System (MerlinTM PCS) Model 3650 is a portable, dedicated programming system designed to interrogate, program, display data, and test St. Jude MedicalTM implantable devices and leads.
FDA Enforcement
Class II
·Terminated·Abbott·April 22, 2020
Smart Stapes Protheses Piston 0.6mm X 4.25 mm- Partial Ossicular Replacement Catalog Number: 70143662
FDA Enforcement
Class II
·Terminated·Olympus Corporation of the Americas·August 26, 2020
Smart Stapes Protheses Piston 0.4mm X 5.25 mm- Partial Ossicular Replacement Catalog Number: 70142168
FDA Enforcement
Class II
·Terminated·Olympus Corporation of the Americas·August 26, 2020
St Jude Medical, 10F Fast-Cath Trio" Hemostasis Introducer, REF # 406308, Sterile EO. The Fast-Cath Trio" Hemostasis Introducer consists of the following components: Port hemostasis adapter (3), Sheath (10F Cath-Lock"), dilator (10F) and 0.038 guidewire. See product labeling for diagram of contents.
FDA Enforcement
Class II
·Terminated·St Jude Medical·October 29, 2014
GORE¿ EXCLUDER¿ Iliac Branch Endoprosthesis (IBE)
FDA Enforcement
Class II
·Terminated·W. L. Gore & Associates Inc.·February 12, 2020
Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the peripheral visual field of a patient. The device projects light on various points of a curved surface, and the patient indicates whether he or she sees the light.
FDA Enforcement
Class II
·Terminated·Haag-Streit USA Inc·September 26, 2012
PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath PINNACLE¿ TIF TIP" Introducer Sheath PINNACLE¿ R/O II Radiopaque Marker Introducer Sheath
FDA Enforcement
Class II
·Terminated·Terumo Medical Corporation·September 14, 2016
Xoran Minicat00202
FDA Enforcement
Class II
·Terminated·Xoran Technologies, Inc.·November 6, 2013
Optilite Freelite Lambda Free Kit Product Code: LK018.OPT, LK018.OPT.A Protein testing kit.
FDA Enforcement
Class II
·Terminated·The Binding Site Group, Ltd.·January 25, 2017
Xoran Minicat00158
FDA Enforcement
Class II
·Terminated·Xoran Technologies, Inc.·November 6, 2013
UltraFill DBM labeled in part: TISSUENET Sterilized by T10^6 Description: UltraFill DBM Size: 5cc Product Code: RT53005 Donated Human Tissue Allograft SINGLE PATIENT USE ONLY FOR INTERNATIONAL USE ONLY See Package Insert for Additional Information TissueNet's Porcine DBM product line is used as a bone void filler.
FDA Enforcement
Class II
·Terminated·Surgical Tissue Network, Inc.·January 16, 2013
UltraFill DBM labeled in part: TISSUENET Sterilized by T10^6 Description: UltraFill DBM Size: 10cc Product Code: RT53010 Donated Human Tissue Allograft SINGLE PATIENT USE ONLY FOR INTERNATIONAL USE ONLY See Package Insert for Additional Information TissueNet's Porcine DBM product line is used as a bone void filler.
FDA Enforcement
Class II
·Terminated·Surgical Tissue Network, Inc.·January 16, 2013
Ultrafill DBM labeled in part: TISSUENET Sterilized by T10^6 Description: UltraFill DBM Size: 1cc Product Code: RT53001 Donated Human Tissue Allograft SINGLE PATIENT USE ONLY FOR INTERNATIONAL USE ONLY See Package Insert for Additional Information TissueNet's Porcine DBM product line is used as a bone void filler
FDA Enforcement
Class II
·Terminated·Surgical Tissue Network, Inc.·January 16, 2013
Esophagoscope Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Esophagus, Stomach and Duodenum. The instrument is introduced via the mouth when indications consistent with the need for procedure are observed in adult and pediatric patient populations.
FDA Enforcement
Class II
·Terminated·Pentax Medical Company·July 6, 2016
Xoran MiniCAT CT Scanner
FDA Enforcement
Class II
·Terminated·Xoran Technologies, Inc.·November 6, 2013
Xoran Mini CT Scanner
FDA Enforcement
Class II
·Terminated·Xoran Technologies, Inc.·November 6, 2013
TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 LEFTTriathlon Femoral Distal Augments are used with Triathlon TS Femoral Components during revision Total Knee Arthroplasty (TKA) and with Triathlon Primary PS Femoral Components during TKA to address distal femoral defects. (See attached IFU (IFU_Triathlon Total Knee_QIN 4376 Rev AB) Catalog # 5542-A-201 - Product Usage:
FDA Enforcement
Class II
·Terminated·Howmedica Osteonics Corp.·October 9, 2019
Giraffe Incubator The Giraffe Incubator is an infant incubator. Incubators provide heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Incubators provide an enclosed temperature controlled environment
FDA Enforcement
Class II
·Terminated·Ohmeda Medical·March 29, 2017
Giraffe Spot PT Ohmeda Medical Spot PT Lite Phototherapy System- The Spot PT Lite Phototherapy System provides light therapy for the treatment of hyperbilirubinemia, commonly known as neonatal jaundice, during the newborn period in the hospital
FDA Enforcement
Class II
·Terminated·Ohmeda Medical·March 29, 2017