37 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DYMEDIX REUSABLE RESPIRATORY EFFORT BELT SENSOR, MODEL 6015 AND DYMEDIX REUSABLE LIMB MOVEMENT SENSOR, MODEL 3100
FDA 510(k)
FDA Class 2
·Anesthesiology
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481123702·LOCATOR R-Tx Attachment System, Straumann Tissu...
LOCATOR F-Tx
FDA UDI
Zest Anchors, LLC·00840481123481·LOCATOR F-Tx Abutment for Regular Neck (RN) Con...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659208445·Kirschner w.trocar point, d/e _x000D_...
Kirschner w.trocar point, d/e 0.7mm/23cm
FDA UDI
mahe medical gmbh·EMAH00406050070·Kirschner w.trocar point, d/e
0.7mm/...
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481128509·LOCATOR R-Tx Abutment, Straumann Tissue Level, ...
ATLAST DATA MANAGEMENT SOFTWARE (DMS)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
STACKHOUSE LENS HOOD, MODEL SA-700/F
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·April 15, 2025
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·June 27, 2025
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·February 22, 2025
EVIS LUCERA ELITE COLONOVIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDF·January 22, 2026
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·March 12, 2025
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·March 12, 2025
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·March 12, 2025
PRIME 5TH WHEEL STRETCHER, 26"
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·April 8, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 22, 2011
ONE TOUCH ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·May 9, 2008
ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·December 29, 2015
LDX V2 ANALYZER NORTH AMERICAN VERSION
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code JJE·September 26, 2023