Stick Tech , Ltd.: FDA clearances and approvals

Stick Tech , Ltd. has 9 FDA 510(k) clearances (first 2001, latest 2006), across 4 product codes in 1 review panel. Median 510(k) review time: 92 days.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
EBIResin, Denture, Relining, Repairing, Rebasing66
DYWBracket, Plastic, Orthodontic11
EBFMaterial, Tooth Shade, Resin11
ELRPost, Root Canal11

Review panels

Most recent Stick Tech , Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K051953EVERSTICK A&ODYW2006-03-21246
K031341STICK FLOWEBF2003-10-29184
K030820EVERSTICK POSTELR2003-05-2067
K030072EVERSTICK PERIOEBI2003-04-1092
K021126EVERSTICK ORTHOEBI2002-05-1335
K011799EVERSTICKNETEBI2001-11-05150
K011788EVERSTICKEBI2001-11-05150
K003334STICK NETEBI2001-01-0875
K003333STICKEBI2001-01-0471

Recalls

openFDA lists no recalls under a recalling firm named Stick Tech , Ltd..

Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.

Frequently asked questions

How many FDA 510(k) clearances does Stick Tech , Ltd. have?

Stick Tech , Ltd. has 9 FDA 510(k) clearances (first 2001, latest 2006), across 4 product codes in 1 review panel.

How long does FDA take to clear Stick Tech , Ltd.'s 510(k)s?

The median time from FDA receipt to decision across Stick Tech , Ltd.'s cleared 510(k)s is 92 days.

What devices does Stick Tech , Ltd. make?

Its most frequent FDA product codes are EBI (Resin, Denture, Relining, Repairing, Rebasing, 6); DYW (Bracket, Plastic, Orthodontic, 1); EBF (Material, Tooth Shade, Resin, 1).

Has Stick Tech , Ltd. had device recalls?

openFDA lists no recalls under a recalling firm name matching Stick Tech , Ltd. Related entities may recall under other names.

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.

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