Jon-Ko Products, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Jon-Ko Products, Inc.” (first 1995, latest 1995), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 312 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
ECIBand, Elastic, Orthodontic44
DZDTube, Orthodontic11

Review panels

Most recent Jon-Ko Products, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K943419ORTHODONTIC ELASTOMERIC LAGATURE MODULEECI1995-05-24313
K943421ORTHODONITC ELASTOMERIC SLEEVINGDZD1995-05-23312
K943420ORTHODONTIC ELASTOMERIC CHAINECI1995-05-23312
K943418ORTHODONTIC ELASTOMERIC SEPARATOR MODULEECI1995-05-23312
K943417ORTHODONTIC ELASTOMERIC TUBE/THREADECI1995-05-23312

Recalls

openFDA lists no recalls under a recalling firm named Jon-Ko Products, 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 Jon-Ko Products, Inc.?

FDA lists 5 510(k) clearances under the applicant name “Jon-Ko Products, Inc.” (first 1995, latest 1995), across 2 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 Jon-Ko Products, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Jon-Ko Products, Inc. is 312 days.

Which FDA product codes appear under Jon-Ko Products, Inc.?

The most frequent FDA product codes under this applicant name are ECI (Band, Elastic, Orthodontic, 4); DZD (Tube, Orthodontic, 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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