15 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Tahoe Uni Knee System
FDA 510(k)
FDA Class 2
·Orthopedic
Oticon
FDA UDI
Oticon A/S·05707131318749·OPN 2, MRITE 312 2.4G NFM PB C094
LIV BREAST SELF EXAMINATION AID
FDA 510(k)
FDA Class 2
·Radiology
DIMENSION VISTA LOCI CA 15-3 FLEX REAGENT CARTRIDGE, DIMENSION VISTA LOCI 7 CALIBRATOR, MODELS: K6456 AND KC605
FDA 510(k)
FDA Class 2
·Immunology
MULTI-LINK RX VISION CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code MAF·June 14, 2013
BARD-PARKER
FDA Adverse Event
Injury
·ASPEN SURGICAL PRODUCTS, INC.·Product code GES·September 30, 2014
GYNECARE MORCELLEX TISSUE MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code HET·September 11, 2008
AMPLATZER AMULET
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NGV·September 25, 2024
(17-0344) ANK IMPL A11 D3.5 MM/L11 MM(IMPLANTS)
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·June 19, 2021
(17-0344) ANK IMPL A11 D3.5 MM/L11 MM(IMPLANTS)
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 3, 2021
(17-0344) ANK IMPL A11 D3.5 MM/L11 MM(IMPLANTS)
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·June 18, 2021
(17-0344) ANK IMPL A11 D3.5 MM/L11 MM(IMPLANTS)
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·June 3, 2021
(17-0344) ANK IMPL A11 D3.5 MM/L11 MM(IMPLANTS)
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 3, 2021
(17-0344) ANK IMPL A11 D3.5 MM/L11 MM(IMPLANTS)
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·June 3, 2021
(17-0344) ANK IMPL A11 D3.5 MM/L11 MM(IMPLANTS)
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·June 18, 2021