Ranir/Dcp Corp.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Ranir/Dcp Corp.” (first 1992, latest 1995), across 4 product codes in 1 review panel. Median 510(k) review time under this name: 168 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

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Top product codes

Product codeDeviceSubmissions510(k) clearances
JESFloss, Dental33
EAXMirror, Mouth11
EFWToothbrush, Manual11
JEQToothbrush, Powered11

Review panels

Most recent Ranir/Dcp Corp. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K955530RANIR HI-TECHNOLOGY DENTAL FLOSSEFW1995-12-2824
K942690RANIR DENTAL TAPE MINT WAXED WITH FLUORIDEJES1995-04-27324
K942689RANIR DENTAL FLOSS MINT WAXED WITH FLUORIDEJES1995-04-27324
K935906RANIR PLAX RXEAX1994-09-02266
K935522RANIR DENTAL TAPE MINT WAXED WITH FLOURIDEJES1994-01-2671
K924739THE DENTIST'S TOOTH POLISHERJEQ1992-11-2463

Recalls

openFDA lists no recalls under a recalling firm named Ranir/Dcp Corp..

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 Ranir/Dcp Corp.?

FDA lists 6 510(k) clearances under the applicant name “Ranir/Dcp Corp.” (first 1992, latest 1995), across 4 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 Ranir/Dcp Corp.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Ranir/Dcp Corp. is 168 days.

Which FDA product codes appear under Ranir/Dcp Corp.?

The most frequent FDA product codes under this applicant name are JES (Floss, Dental, 3); EAX (Mirror, Mouth, 1); EFW (Toothbrush, Manual, 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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