Yorktowne Optical Co., Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Yorktowne Optical Co., Inc.” (first 1990, latest 1994), across 1 product code in 1 review panel. Median 510(k) review time under this name: 57 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

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Top product codes

Product codeDeviceSubmissions510(k) clearances
HQYSunglasses (Non-Prescription Including Photosensitive)55

Review panels

Most recent Yorktowne Optical Co., Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K935446VISUAL HEALTHSHIELDSHQY1994-02-1797
K904585POST MYDRIATIC SPECTACLESHQY1990-10-2617
K903721WRAP-AROUND INSTANT SUNGLASSESHQY1990-10-1157
K903720FLAT FIT-IN SUNGLASSESHQY1990-10-1157
K903719FLAT SLIP-IN SUNGLASSESHQY1990-10-1157

Recalls

openFDA lists no recalls under a recalling firm named Yorktowne Optical Co., Inc..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Frequently asked questions

How many FDA 510(k) clearances are listed under Yorktowne Optical Co., Inc.?

FDA lists 5 510(k) clearances under the applicant name “Yorktowne Optical Co., Inc.” (first 1990, latest 1994), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Yorktowne Optical Co., Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Yorktowne Optical Co., Inc. is 57 days.

Which FDA product codes appear under Yorktowne Optical Co., Inc.?

The most frequent FDA product codes under this applicant name are HQY (Sunglasses (Non-Prescription Including Photosensitive), 5).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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