2,431 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Ref/Keratometers HRK-7000
FDA UDI
Huvitz Co., Ltd.·08800019600138·The Ref/Keratometer is intended to be used to m...
Ref-Keratometer HRK-1
FDA UDI
Huvitz Co., Ltd.·08800019600480·The Ref/Keratometer is intended to be used to m...
Auto Ref-Keratometer HRK-8000A
FDA UDI
Huvitz Co., Ltd.·08800019600152·The Auto Ref/Keratometer is intended to be used...
Auto Ref-Keratometer HRK-9000A
FDA UDI
Huvitz Co., Ltd.·08800019600169·The Auto Ref/Keratometer is intended to be used...
Auto Ref/Keratometer HRK-8100A
FDA UDI
Huvitz Co., Ltd.·08800019600923·Auto Ref/Keratometer HRK-8100A is intended to p...
Auto Ref-Keratometer HRK-7000A
FDA UDI
Huvitz Co., Ltd.·08800019600145·The Auto Ref/Keratometer is intended to be used...
HRK-63-16 KNEE ARRAY COIL, HRK-127-16 KNEE ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
MODELS HRK-63-8 PMS AND HRK-127-8 KNEE ARRAY COILS
FDA 510(k)
FDA Class 2
·Radiology
HRK-63 KNEE ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
HRK-123 KNEE ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
HRK-63-8 KNEE ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
*
FDA Adverse Event
Injury
·BAUSCH-LOMB STORZ INSTRUMENT CO.·Product code HRK·March 10, 2004
VAS HD AC 4MM X 30 DEG
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code HRK·May 14, 2020
SCRAPER MEMBRANE DIAMOND DUST
FDA Adverse Event
Injury
·SYNERGETICS CORP.·Product code HRK·July 12, 2016
Table, Instrument, Manual, Ophthalmic
FDA classification
FDA Class 1
·Table, Instrument, Manual, Ophthalmic
ARK SURGICAL
FDA registration
ARK SURGICAL·2 products·🇮🇱 Israel
HPK INDUSTRIES
FDA registration
HPK INDUSTRIES·5 products·🇺🇸 United States
Beautifil Flow Plus/Super Snap
FDA UDI
SHOFU DENTAL CORPORATION·E235ARK0·Attchment Removal Kit for Clear Aligners. Conta...
ARK DIAGNOSTICS INC
FDA registration
ARK DIAGNOSTICS INC·19 products·🇺🇸 United States
LERADO H.K. LTD.
FDA registration
LERADO H.K. LTD.·15 products·🇨🇳 China