American Dent-All, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “American Dent-All, Inc.” (first 2000, latest 2003), across 1 product code in 1 review panel. Median 510(k) review time under this name: 60 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
EJHAlloy, Metal, Base55

Review panels

Most recent American Dent-All, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K030161SUPERBONDEJH2003-03-1760
K011706FLEXICAST PRIMEEJH2001-08-0663
K011705SUPREMCASTEJH2001-08-0360
K003509FLEXICASTEJH2001-01-0249
K001383SUPREMCAST VEJH2000-07-0564

Recalls

openFDA lists no recalls under a recalling firm named American Dent-All, 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.

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

How many FDA 510(k) clearances are listed under American Dent-All, Inc.?

FDA lists 5 510(k) clearances under the applicant name “American Dent-All, Inc.” (first 2000, latest 2003), 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 American Dent-All, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name American Dent-All, Inc. is 60 days.

Which FDA product codes appear under American Dent-All, Inc.?

The most frequent FDA product codes under this applicant name are EJH (Alloy, Metal, Base, 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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