The Emerging Technologies Group: FDA filings under this applicant name

FDA lists 7 510(k) clearances under the applicant name “The Emerging Technologies Group” (first 1996, latest 1997), across 1 product code in 1 review panel. Median 510(k) review time under this name: 190 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
DZEImplant, Endosseous, Root-Form77

Review panels

Most recent The Emerging Technologies Group 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K961381KIS-III NON-SUBMERGED IMPLANT, SCREWS AND CYLINDERSDZE1997-09-09539
K961387MT-XDZE1996-09-25190
K961386MT-2ADZE1996-09-25190
K961385MT-3ADZE1996-09-25190
K961384MT-2DZE1996-09-25190
K961383MT1DZE1996-09-25190
K961382MT1ADZE1996-09-25190

Recalls

openFDA lists no recalls under a recalling firm named The Emerging Technologies Group.

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 The Emerging Technologies Group?

FDA lists 7 510(k) clearances under the applicant name “The Emerging Technologies Group” (first 1996, latest 1997), 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 The Emerging Technologies Group?

The median time from FDA receipt to decision across 510(k)s cleared under the name The Emerging Technologies Group is 190 days.

Which FDA product codes appear under The Emerging Technologies Group?

The most frequent FDA product codes under this applicant name are DZE (Implant, Endosseous, Root-Form, 7).

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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