27 results
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44ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ZELTIQ COOLSCULPTING
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ACRY PLUS V.
FDA UDI
DENTAL MANUFACTURING SPA·08056865012230·
LEONE SPA
FDA UDI
LEONE SPA·08033707008859·CALIBRA 1ST MOLAR BANDS n.UR 23
MIRABAY
FDA UDI
Mirabay Orthodontics Corp.·05061075023245·KLEOS 2 PSL METAL HIGH TORQUE 022 UL45 HK PK5
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810057372179·Finger Trap Large
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·KAMRA INLAY
NA
FDA UDI
STRYKER CORPORATION·04546540078476·9.5mm x 10.4mm Boring Tool
NA
FDA UDI
STRYKER CORPORATION·04546540078452·12.6mm x 10.4mm Boring Tool
NA
FDA UDI
STRYKER CORPORATION·04546540078469·15.6mm x 10.4mm Boring Tool
DAKO MONOCLONAL MOUSE ANTI-HUMAN PROGESTERONE RECEPTOR, CLONE PGR 636, ANTIBODY FOR IMMUNOENZYMATIC STAINING
FDA 510(k)
FDA Class 2
·Hematology
PROFILE-V MEDTOXSCAN DRUGS OF ABUSE TEST SYSTEM AND 12 DRUGS TEST SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Toxicology
COVIDIEN 14 FRENCH SILICONE COUDE FOLEY
FDA Adverse Event
Injury
·CARDINAL HEALTH·Product code KOD·November 6, 2023
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·KAMRA INLAY
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·KAMRA INLAY
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·KAMRA INLAY
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·KAMRA INLAY
V.A.C. FREEDOM THERAPY SYSTEM
FDA Adverse Event
Injury
·KINETIC CONCEPTS, INC.·Product code OMP·February 15, 2021
LEAD MODEL UNKNOWN
FDA Adverse Event
Injury
·CYBERONICS INC·Product code LYJ·May 20, 2013
ADVANTAGE SERIES 26 OBS
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·May 26, 2011
COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code HQL·August 14, 2008