13 results
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24ms
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Sources: EU EUDAMED, US FDA
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Country: United States
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APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690196440·AK3 Ultra Tibial Insert Trials Size 1 - 5 Pan
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101063·KNAPP RETRACTOR 4-PRONG SHARP
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690195153·AK3 Ultra Tibial Insert Trials Size 1 - 5 Pan I...
ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·June 7, 2013
PLUS SL
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS AG·Product code KWY·October 7, 2008
LINOX SD 65/16
FDA Adverse Event
Malfunction
·BIOTRONIK, SE & CO KG·Product code LWS·June 29, 2011
HF-RESECTION ELECTRODE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023
TELESCOPE, 3 MM, 30°, WIDEANGLE, AUTOCLAVABLE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·April 25, 2023
HF-RESECTION ELECTRODE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023
HANDPIECE, EMAX 2 PLUS (ANSPACH DRILL), ROHS COMPLIANT
FDA Adverse Event
Injury
·BLUE BELT TECHNOLOGIES·Product code HBE·April 23, 2020
HANDPIECE, EMAX 2 PLUS (ANSPACH DRILL), ROHS COMPLIANT
FDA Adverse Event
Injury
·BLUE BELT TECHNOLOGIES·Product code HBE·April 24, 2020