12 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VenaCure EVLT NeverTouch Procedure Kit
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FEMORAL CENTERING SLEEVE
FDA UDI
Biomet Orthopedics, LLC·00880304254183·
SCHWERT
FDA UDI
A. Schweickhardt GmbH & Co. KG·E89611629140·TC-Needle holder OLSEN-HEGAR 14 cm
TQ HBA1C GEN3
FDA 510(k)
FDA Class 2
·Hematology
HEM-O-LOK LIGATION CLIP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
UNKNOWN PLATE
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·April 21, 2026
UNKNOWN PLATE
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·April 21, 2026
UNKNOWN PLATE
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·April 21, 2026
VITATRON DA+ C-SERIES SR
FDA Adverse Event
Malfunction
·IPG MFG SWITZERLAND·Product code DXY·October 10, 2014
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·May 13, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011
Optical Access System; 5mm x 100mm and 12mm x 100mm; Model #: CTR03 and CTR73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal procedures.
FDA Enforcement
Class II
·Terminated·Stryker Sustainability Solutions·July 1, 2015