45 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ROMIAPEX MODEL A-15
FDA 510(k)
FDA Unclassified
·Unknown
Bur PM2-95 80K Diamond coarse Ø2.0 sterile
FDA UDI
Bien-Air Surgery SA·17630055514216·
Zavation
FDA UDI
Zavation LLC·00842166182226·Drill Guide
OsteoMed
FDA UDI
OSTEOMED LLC·00845694033404·Lone Surgeon Plate, 60 Degree, Mini, 4Hole, Long
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704598865·TRAY STAINLESS STEEL 13" X 20.25" X 3.5"
PILLING
FDA UDI
TELEFLEX INCORPORATED·14026704730329·
KRATZ-BARRAQUER WIRE SPECULUM
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896072138·KRATZ BARRAQUER WIRE SPECULUM INFANT SIZE OPEN ...
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100540·Caddie, 8.5mm Screws
RADS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
FIXCET SPINAL FACET SCREW SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523127566·Acetabular Trial Shell, 54mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523127801·Universal Acetabular Trial Shell, 54mm
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 10, 2020
V200 / ESPRIT
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 5, 2018
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·May 20, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 7, 2021
V200 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 9, 2020