Volk Optical, Inc.
Volk Optical, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2015, with 4 FDA device recalls on record.
Top product codes for Volk Optical, Inc.
FDA recalls by Volk Optical, Inc.
- Z-1177-2016 — 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
- Z-1685-2015 — 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.
- Z-2055-2015 — Lombart 90D Clear with case Visualization during diagnosis and laser therapy of the human retina (fundus) using a slit lamp.
- Z-0966-2013 — 20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens For visualization during diagnosis and laser therapy of the human retina (fundus) using a binocular indirect ophthalmoscope.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Volk Optical, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.