31 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CONSENSUS UNIPOLAR HEAD, COCR
FDA 510(k)
FDA Class 2
·Orthopedic
SourceLink™
FDA UDI
Bard Brachytherapy, Inc.·10801741078146·0.5mm Seed-to-Seed SourceLink™ Connectors
Endocervical Speculum Blue Titanium
FDA UDI
MEDGYN PRODUCTS, INC.·M803030205·Endocervical Speculum Blue Titanium
Holder, Needle, Micro, Jacobson/catch round-handle 21cm tip 0.8mm
FDA UDI
Geister Medizintechnik GmbH·04057034005477·Holder, Needle, Micro, Jacobson/catch
round-...
Unigraft
FDA UDI
UNICARE BIOMEDICAL INC.·D767U0302051·Unigraft is made of synthetic bioactive glass m...
EMBRYON SINGLE AND DOUBLE LUMEN NEEDLES
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
TRANSFX ANGLED RODS
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·February 4, 2025
CLAREON ASPHERIC UV ABSORBING IOL WITH AUTONOME DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·ALCON LABORATORIES IRELAND LTD.·Product code HQL·September 12, 2025
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 12, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 2, 2018
SOFPORT ADVANCED OPTIC LENS
FDA Adverse Event
Injury
·BAUSCH AND LOMB·Product code HQL·March 27, 2013
8800
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·March 7, 2011
UNK DEPUY INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HSH·April 16, 2008
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·June 21, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·June 21, 2011
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 29, 2016