Med Mart, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Med Mart, Inc.” (first 1993, latest 1994), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 53 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
INQTable, Powered44
INWTable, Mechanical11

Review panels

Most recent Med Mart, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K941281OCCUPATIONAL THERAPY TABLESINQ1994-05-0651
K940131TABLE MAT MORTORIZED/ELECTRICINQ1994-02-2553
K932749MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLEINQ1993-07-2244
K932412TREATMENT TABLES, ELECTRICALLY ACTIVATEDINQ1993-07-21111
K931635TREATMENT TABLES, MANUALLY ACTIVATEDINW1993-07-21111

Recalls

openFDA lists no recalls under a recalling firm named Med Mart, 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 Med Mart, Inc.?

FDA lists 5 510(k) clearances under the applicant name “Med Mart, Inc.” (first 1993, latest 1994), across 2 product codes 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 Med Mart, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Med Mart, Inc. is 53 days.

Which FDA product codes appear under Med Mart, Inc.?

The most frequent FDA product codes under this applicant name are INQ (Table, Powered, 4); INW (Table, Mechanical, 1).

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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