Kreativ, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Kreativ, Inc.” (first 1994, latest 2000), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 274 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
KOJAirbrush33
EBFMaterial, Tooth Shade, Resin11
EIEDam, Rubber11

Review panels

Most recent Kreativ, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K990060MACH 7KOJ2000-06-15524
K983227POWER BLOCKEIE1998-12-1187
K980216KREATIV MACH 5, MACH 5 PLUS, MACH M, MACH 6KOJ1998-06-16146
K962376KREATIV KURING LIGHT SYSTEMEBF1997-03-21274
K940776KREATIV MODEL KV-1KOJ1994-12-21302

Recalls

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

FDA lists 5 510(k) clearances under the applicant name “Kreativ, Inc.” (first 1994, latest 2000), 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 Kreativ, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Kreativ, Inc. is 274 days.

Which FDA product codes appear under Kreativ, Inc.?

The most frequent FDA product codes under this applicant name are KOJ (Airbrush, 3); EBF (Material, Tooth Shade, Resin, 1); EIE (Dam, Rubber, 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 (spelling variants such as punctuation and legal suffixes combined); 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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