8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
MRX-280
FDA 510(k)
FDA Class 2
·Radiology
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110997·DOUBLE PLASTIC STERILIZATION CASE
Monkey Rings External Fixation System
FDA UDI
Paragon 28, Inc.·00889795115263·Wire, Ø2.0 x 400 Smooth, Half Point
OCS-B COLLAGEN
FDA 510(k)
FDA Class 2
·Dental
TRIACTIV SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
SILVERT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYB·February 4, 2013
SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INRAOCULA
FDA Adverse Event
Malfunction
·STAAR SURGICAL CO.·Product code HQL·November 9, 2010
ASPHERE M SPEC 12/14 36 -2
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·July 17, 2014