Neirynck & Vogt NV: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Neirynck & Vogt NV” (first 2002, latest 2002), across 1 product code in 1 review panel. Median 510(k) review time under this name: 43 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
EJHAlloy, Metal, Base55

Review panels

Most recent Neirynck & Vogt NV 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K023477BIOLOYEJH2002-12-1358
K021971CERALOYEJH2002-08-0145
K021969CHROLOYEJH2002-07-3043
K021968CERALOY SOLDEREJH2002-07-2639
K021965CHROLOY SOLDEREJH2002-07-2639

Recalls

openFDA lists no recalls under a recalling firm named Neirynck & Vogt NV.

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 Neirynck & Vogt NV?

FDA lists 5 510(k) clearances under the applicant name “Neirynck & Vogt NV” (first 2002, latest 2002), 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 Neirynck & Vogt NV?

The median time from FDA receipt to decision across 510(k)s cleared under the name Neirynck & Vogt NV is 43 days.

Which FDA product codes appear under Neirynck & Vogt NV?

The most frequent FDA product codes under this applicant name are EJH (Alloy, Metal, Base, 5).

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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