7,774 results · 28ms · Sources: EU EUDAMED, 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