Maurry Biological Co.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Maurry Biological Co.” (first 1985, latest 1986), across 1 product code in 1 review panel. Median 510(k) review time under this name: 96 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

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Top product codes

Product codeDeviceSubmissions510(k) clearances
HPXLens, Contact (Polymethylmethacrylate)66

Review panels

Most recent Maurry Biological Co. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K861712WETTING & SOAKING HARD CONTACT LENS SOLUTIONHPX1986-05-2924
K853809DAILY HARD CONTACT LENS CLEANERHPX1986-03-11181
K853808HARD CONTACT LENS CLEANING & SOAKING SOLUTIONHPX1986-03-11181
K853811HARD CONTACT LENS SOAKING SOLUTIONHPX1985-12-1696
K853810WETTING SOLUTION FOR HARD CONTACT LENSESHPX1985-12-1696
K853807ALL-IN-ONE HARD CONTACT LENS SOLUTIONHPX1985-12-1696

Recalls

openFDA lists no recalls under a recalling firm named Maurry Biological Co..

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 Maurry Biological Co.?

FDA lists 6 510(k) clearances under the applicant name “Maurry Biological Co.” (first 1985, latest 1986), 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 Maurry Biological Co.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Maurry Biological Co. is 96 days.

Which FDA product codes appear under Maurry Biological Co.?

The most frequent FDA product codes under this applicant name are HPX (Lens, Contact (Polymethylmethacrylate), 6).

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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