U.S. Table, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “U.S. Table, Inc.” (first 1995, latest 1995), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 58 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
INQTable, Powered44
ITHEquipment, Traction, Powered11

Review panels

Most recent U.S. Table, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K953621EVT-3300INQ1995-11-14103
K953622PTT 6200 ELEVATION THERAPY TABLEINQ1995-09-1139
K951419FLEX D-4000INQ1995-06-3094
K952600EVT-5000BXINQ1995-06-2216
K951228ASH-7000ITH1995-05-1758

Recalls

openFDA lists no recalls under a recalling firm named U.S. Table, 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 U.S. Table, Inc.?

FDA lists 5 510(k) clearances under the applicant name “U.S. Table, Inc.” (first 1995, latest 1995), 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 U.S. Table, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name U.S. Table, Inc. is 58 days.

Which FDA product codes appear under U.S. Table, Inc.?

The most frequent FDA product codes under this applicant name are INQ (Table, Powered, 4); ITH (Equipment, Traction, Powered, 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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