Matech, Inc.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Matech, Inc.” (first 1994, latest 2001), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 48 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
20120—
20130—
20140—
20150—
20160—
20170—
20180—
20190—
20200—
20210—
20220—
20230—
20240—
20250—
20260—

Top product codes

Product codeDeviceSubmissions510(k) clearances
EJHAlloy, Metal, Base44
ELWMaterial, Impression22

Review panels

Most recent Matech, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K010069DURABOND NON-PRECIOUS CERAMIC ALLOYEJH2001-02-1538
K993572CERADIUM V NON-PRECIOUS CERAMIC ALLOYEJH1999-12-1353
K992881HI BOND NON-PRECIOUS CERAMIC ALLOYEJH1999-11-1985
K992705CERADIUM NON-PRECIOUS CERAMIC ALLOYEJH1999-09-2242
K974894KROMATICA COLOR CHANGING ALGINATEELW1998-02-1243
K925746REPLICAELW1994-01-21434

Recalls

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

FDA lists 6 510(k) clearances under the applicant name “Matech, Inc.” (first 1994, latest 2001), 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 Matech, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Matech, Inc. is 48 days.

Which FDA product codes appear under Matech, Inc.?

The most frequent FDA product codes under this applicant name are EJH (Alloy, Metal, Base, 4); ELW (Material, Impression, 2).

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.

All FDA device companies · FDA product code lookup