The Limited Stores, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “The Limited Stores, Inc.” (first 1991, latest 1994), across 1 product code in 1 review panel. Median 510(k) review time under this name: 66 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

YearClearancesMedian review days
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Top product codes

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

Review panels

Most recent The Limited Stores, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K941875SUNGLASSESHQY1994-06-0346
K910127SUNGLASSES, NON-PRESCRIPTION (POLINELLI)HQY1991-03-1466
K910126SUNGLASSES, NON-PRESCRIPTION (ITALO CREMONA)HQY1991-03-1466
K910125SUNGLASSES/NON-PRESCRIPTION (LA GIARDINIERA)HQY1991-03-1466
K905864SUNGLASSES (NON-PRESCRIPTION)HQY1991-03-1484

Recalls

openFDA lists no recalls under a recalling firm named The Limited Stores, 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 The Limited Stores, Inc.?

FDA lists 5 510(k) clearances under the applicant name “The Limited Stores, Inc.” (first 1991, 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 The Limited Stores, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name The Limited Stores, Inc. is 66 days.

Which FDA product codes appear under The Limited Stores, 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, with punctuation and legal suffixes removed; 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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