Qualis, Inc.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Qualis, Inc.” (first 1997, latest 2005), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 50 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
NUCLubricant, Personal33
HISCondom22
KMJLubricant, Patient11

Review panels

Most recent Qualis, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K050212PERSONAL WARMING JELLYNUC2005-03-1745
K050211PERSONAL WARMING GELNUC2005-03-1745
K041129PERSONAL LUBRICATING GELNUC2004-09-24147
K040085PERSONAL WARMING LUBRICANTHIS2004-04-2095
K973780PERSONAL LUBRICATING LIQUIDHIS1997-11-2654
K973557LUBRIGLIDEKMJ1997-10-1021

Recalls

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

FDA lists 6 510(k) clearances under the applicant name “Qualis, Inc.” (first 1997, latest 2005), across 3 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Qualis, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Qualis, Inc. is 50 days.

Which FDA product codes appear under Qualis, Inc.?

The most frequent FDA product codes under this applicant name are NUC (Lubricant, Personal, 3); HIS (Condom, 2); KMJ (Lubricant, Patient, 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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