Oms Medico, Inc.: FDA filings under this applicant name

FDA lists 7 510(k) clearances under the applicant name “Oms Medico, Inc.” (first 1987, latest 1987), across 1 product code in 1 review panel. Median 510(k) review time under this name: 34 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
GZJStimulator, Nerve, Transcutaneous, For Pain Relief77

Review panels

Most recent Oms Medico, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K874550TX-4(TENS) (SIGMA TENS)GZJ1987-11-2016
K874333TX-2(TENS)GZJ1987-11-2029
K873420GLOBALCARE(TENS)GZJ1987-10-0843
K873484120Z(TENS)GZJ1987-09-1616
K871699TX-3(TENS)GZJ1987-06-2555
K870583NEU-PULS(TENS) MODEL #295GZJ1987-03-1734
K865063UNI-PULS(TENS) MODEL #292GZJ1987-03-1783

Recalls

openFDA lists no recalls under a recalling firm named Oms Medico, 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 Oms Medico, Inc.?

FDA lists 7 510(k) clearances under the applicant name “Oms Medico, Inc.” (first 1987, latest 1987), 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 Oms Medico, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Oms Medico, Inc. is 34 days.

Which FDA product codes appear under Oms Medico, Inc.?

The most frequent FDA product codes under this applicant name are GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief, 7).

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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