Sonacare Medical, LLC: FDA filings under this applicant name

FDA lists 1 510(k) clearance under the applicant name “Sonacare Medical, LLC” (first 2016, latest 2016), plus 1 De Novo decision, across 1 product code in 1 review panel. Median 510(k) review time under this name: 260 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
20161260
20170—
20180—
20190—
20200—
20210—
20220—
20230—
20240—
20250—
20260—

Top product codes

Product codeDeviceSubmissions510(k) clearances
PLPHigh Intensity Ultrasound System For Prostate Tissue Ablation21

Review panels

Most recent Sonacare Medical, LLC 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K160942SonablatePLP2016-12-21260

PMA and De Novo decisions

NumberPathwayDeviceDecision date
DEN150011De NovoHigh Intensity Ultrasound System For Prostate Tissue Ablation2015-10-09

Recalls

openFDA lists no recalls under a recalling firm named Sonacare Medical, LLC.

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 Sonacare Medical, LLC?

FDA lists 1 510(k) clearance under the applicant name “Sonacare Medical, LLC” (first 2016, latest 2016), 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 Sonacare Medical, LLC?

The median time from FDA receipt to decision across 510(k)s cleared under the name Sonacare Medical, LLC is 260 days.

Which FDA product codes appear under Sonacare Medical, LLC?

The most frequent FDA product codes under this applicant name are PLP (High Intensity Ultrasound System For Prostate Tissue Ablation, 2).

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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