Caltech Industries, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Caltech Industries, Inc.” (first 1995, latest 1998), across 1 product code in 1 review panel. Median 510(k) review time under this name: 98 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
LRJDisinfectant, Medical Devices55

Review panels

Most recent Caltech Industries, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K983869DISPATCH HOSPITAL CLEANER DISINFECTANT TOWELS WITH BLEACHLRJ1998-11-3028
K982985CITREX HOSPITAL SPRAY DISINFECTANTLRJ1998-11-0268
K952405CITRACE HOSPITAL GERMICIDAL DEODORIZERLRJ1995-08-2898
K952336DISPATCH HOSPITAL CLEANER DISINFECTANT WITH BLEACHLRJ1995-08-28102
K951512PRECISE HOSPITAL FOAM CLEANER DISINFECTANTLRJ1995-08-07126

Recalls

openFDA lists no recalls under a recalling firm named Caltech Industries, 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 Caltech Industries, Inc.?

FDA lists 5 510(k) clearances under the applicant name “Caltech Industries, Inc.” (first 1995, latest 1998), 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 Caltech Industries, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Caltech Industries, Inc. is 98 days.

Which FDA product codes appear under Caltech Industries, Inc.?

The most frequent FDA product codes under this applicant name are LRJ (Disinfectant, Medical Devices, 5).

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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