16 results
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18ms
·
Sources: EU EUDAMED, US FDA
System Sophi
FDA 510(k)
FDA Class 2
·Ophthalmic
Darby Dental Supply, LLC
FDA UDI
DARBY DENTAL SUPPLY, LLC·00889813058626·STERILE CARBIDE BUR FG701SURG
Cardiovascular Procedure Kit
FDA UDI
Terumo Cardiovascular Systems Corporation·00699753468320·
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481125973·LOCATOR R-Tx Attachment System, 3.5 EC Implants...
Good Works
FDA UDI
Bosma Enterprises·00818634025029·Good Works Performance Pro Small 100/Box
Bradshaw Medical Inc.
FDA UDI
Bradshaw Medical, Inc.·00810019931222·BIT, BLADE SMALL .04" X .19" 1/4 SQ
Zimmer Nexel Total Elbow Ulnar Cement Diverter
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFICATION TO: XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
G7
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 21, 2025
INTERMATE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·November 14, 2014
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·September 15, 2011
GYNECARE GYNEMESH
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·July 26, 2013
250-501 PERFECT CLEAR ∥ STANDARD022
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Osstem Orthodontics Inc.·1 device
Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures. Distributed individually and in kits.
FDA Enforcement
Class II
·Terminated·Applied Medical Resources Corp·May 18, 2016
Achieva 1.5T
FDA Enforcement
Class II
·Ongoing·Philips North America Llc·November 29, 2023
Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in the USA by Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The T2 Arthrodesis Nail is intended for the treatment of Knee Arthrodesis. The design of the T2 Arthrodesis Nail features a unique curvature which incorporates both femur ante curvature and knee valgus bend. Indications: Aseptic failed total knee arthro-plasty with or without bone loss; Failed external fixation, non unions and malunions; Periarticular fractures where repair is not possible; Pathologic fractures and tumor resections; Pseudoarthrosis and correct osteotomy; Ipsilateral femur fractures; and Open and closed femoral fractures.
FDA Enforcement
Class II
·Terminated·Stryker Howmedica Osteonics Corp.·July 25, 2012