G.B.F. Industries, Inc.: FDA clearances and approvals

G.B.F. Industries, Inc. has 5 FDA 510(k) clearances (first 1985, latest 1987), across 3 product codes in 2 review panels. Median 510(k) review time: 28 days.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
JJYMulti-Analyte Controls, All Kinds (Assayed)33
EFQGauze/Sponge, Internal11
NADDressing, Wound, Occlusive11

Review panels

Most recent G.B.F. Industries, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K862565CHEMTROL(TM)JJY1987-01-13190
K862587CHEMTROL(TM)JJY1986-08-0428
K862586CHEMVARION(TM)JJY1986-08-0428
K854850FALKON STRETCH-STERILENAD1986-01-1340
K854432FALKON STRETCHEFQ1985-11-2217

Recalls

openFDA lists no recalls under a recalling firm named G.B.F. Industries, Inc..

Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.

Frequently asked questions

How many FDA 510(k) clearances does G.B.F. Industries, Inc. have?

G.B.F. Industries, Inc. has 5 FDA 510(k) clearances (first 1985, latest 1987), across 3 product codes in 2 review panels.

How long does FDA take to clear G.B.F. Industries, Inc.'s 510(k)s?

The median time from FDA receipt to decision across G.B.F. Industries, Inc.'s cleared 510(k)s is 28 days.

What devices does G.B.F. Industries, Inc. make?

Its most frequent FDA product codes are JJY (Multi-Analyte Controls, All Kinds (Assayed), 3); EFQ (Gauze/Sponge, Internal, 1); NAD (Dressing, Wound, Occlusive, 1).

Has G.B.F. Industries, Inc. had device recalls?

openFDA lists no recalls under a recalling firm name matching G.B.F. Industries, Inc. Related entities may recall under other names.

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.

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