7,774 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DISPOSABLE VITRECTOMY LENS: MAGNIFYING
FDA Adverse Event
Malfunction
·DUTCH OPHTHALMIC USA·Product code HJK·July 8, 2020
DISPOSABLE VITRECTOMY LENS: FLAT
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER INT.·Product code HJK·September 15, 2020
RXSIGHT CONTACT LENS
FDA Adverse Event
Injury
·RXSIGHT, INC.·Product code HJK·August 8, 2025
RXSIGHT CONTACT LENS
FDA Adverse Event
Injury
·RXSIGHT INC.·Product code HJK·January 8, 2026
RXSIGHT CONTACT LENS
FDA Adverse Event
Injury
·RXSIGHT INC.·Product code HJK·January 8, 2026
DISPOSABLE VITRECTOMY LENS: WIDE VIEW
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code HJK·October 11, 2019
DISPOSABLE VITRECTOMY LENS: FLAT
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code HJK·December 18, 2019
DISPOSABLE VITRECTOMY LENS: WIDE VIEW
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code HJK·October 7, 2019
Volk 25D Large Clear BIO Lens with case UPC: 8 11608 01010 6, VOLK OPTICAL INC. The Volk Optical BIO Lenses are intended for visualization during diagnosis and laser therapy of the human retina (fundus) using a binocular indirect ophthalmoscope.
FDA Recall
Terminated
·Volk Optical Inc·Product code HJK·February 27, 2015
Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk Magnifying Lens, Catalog VMD
FDA Recall
Open, Classified
·Vortex Surgical Inc.·Product code HJK·December 16, 2025
Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602 for use as diagnostic contact lenses for eye examinations (including the anterior chamber, trabecular meshwork, central retina, and peripheral retina) and use in the therapy of intraocular abnormalities
FDA Recall
Terminated
·Volk Optical Inc·Product code HJK·February 2, 2016
Lens, Contact, Polymethylmethacrylate, Diagnostic
FDA classification
FDA Class 2
·Lens, Contact, Polymethylmethacrylate, Diagnostic
CAPTURE-R READY-SCREEN 3
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·April 21, 2016
HPK INDUSTRIES
FDA registration
HPK INDUSTRIES·5 products·🇺🇸 United States
HEK
FDA 510(k)
FDA Class 1
·Hematology
HEK
FDA 510(k)
FDA Class 1
·Hematology
HEK GENCELLS
FDA 510(k)
FDA Class 1
·Hematology
LERADO H.K. LTD.
FDA registration
LERADO H.K. LTD.·15 products·🇨🇳 China
AZAD INTERNATIONAL (H.K.) LTD.
FDA registration
AZAD INTERNATIONAL (H.K.) LTD.·6 products·🇭🇰 Hong Kong
HJD CALCAR REPLACEMENT PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic