Soclean, Inc.: FDA filings under this applicant name

FDA lists 1 510(k) clearance under the applicant name “Soclean, Inc.” (first 2025, latest 2025), plus 1 De Novo decision, across 1 product code in 1 review panel. Median 510(k) review time under this name: 303 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
20251303
20260—

Review time against the same product codes

Since 2017, 510(k)s cleared under the name Soclean, Inc. took a median 303 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 284 days.

Top product codes

Product codeDeviceSubmissions510(k) clearances
QXQRespiratory Accessory Microbial Reduction Device.21

Review panels

Most recent Soclean, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K243815SoClean 3+QXQ2025-10-10303

PMA and De Novo decisions

NumberPathwayDeviceDecision date
DEN210037De NovoRespiratory Accessory Microbial Reduction Device.2024-08-12

Recalls

2 product recalls in 1 recall events; 2 initiated in the last five years. Most recent: 2023-11-15.

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 Soclean, Inc.?

FDA lists 1 510(k) clearance under the applicant name “Soclean, Inc.” (first 2025, latest 2025), 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 Soclean, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Soclean, Inc. is 303 days.

Which FDA product codes appear under Soclean, Inc.?

The most frequent FDA product codes under this applicant name are QXQ (Respiratory Accessory Microbial Reduction Device., 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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