Possum, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Possum, Inc.” (first 1977, latest 1977), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 6 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
ILQSystem, Communication, Powered33
ILPSystem, Communication, Non-Powered11
IQASystem, Environmental Control, Powered11

Review panels

Most recent Possum, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K770032PAGE TURNERILP1977-01-126
K770031ALARM INTERCOM DOOR LOCKILQ1977-01-126
K770030ALARM, COMMUN.-SEC. INDEP.-EMER.ILQ1977-01-126
K770029TYPEWRITER CONTROL SYSTEMSILQ1977-01-126
K770028ENVIRONMENTAL CONTROL SYSTEMSIQA1977-01-126

Recalls

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

FDA lists 5 510(k) clearances under the applicant name “Possum, Inc.” (first 1977, latest 1977), across 3 product codes 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 Possum, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Possum, Inc. is 6 days.

Which FDA product codes appear under Possum, Inc.?

The most frequent FDA product codes under this applicant name are ILQ (System, Communication, Powered, 3); ILP (System, Communication, Non-Powered, 1); IQA (System, Environmental Control, Powered, 1).

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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