Barnev, Ltd.: FDA filings under this applicant name

FDA lists 2 510(k) clearances under the applicant name “Barnev, Ltd.” (first 2008, latest 2009), plus 1 De Novo decision, across 1 product code in 1 review panel. Median 510(k) review time under this name: 118 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
NPBSystem, Monitoring, For Progress Of Labor32

Review panels

Most recent Barnev, Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K082704BIRTHTRACK (A.K.A. CLM)NPB2009-01-09115
K080672BIRTHTRACKNPB2008-07-08120

PMA and De Novo decisions

NumberPathwayDeviceDecision date
DEN060006De NovoSystem, Monitoring, For Progress Of Labor2007-01-30

Recalls

openFDA lists no recalls under a recalling firm named Barnev, Ltd..

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 Barnev, Ltd.?

FDA lists 2 510(k) clearances under the applicant name “Barnev, Ltd.” (first 2008, latest 2009), plus 1 De Novo decision, 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 Barnev, Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Barnev, Ltd. is 118 days.

Which FDA product codes appear under Barnev, Ltd.?

The most frequent FDA product codes under this applicant name are NPB (System, Monitoring, For Progress Of Labor, 3).

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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