510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K053383Substantially Equivalent

Fidis Celiac

Biomedical Diagnostics (Bmd) SA, Marne La Vallee Cedex 2, FR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K053383 is the FDA 510(k) clearance record for FIDIS CELIAC, a class II device, cleared for Biomedical Diagnostics (Bmd) SA on under FDA product code MST (Antibodies, Gliadin). FDA records list 10 510(k) clearances for Biomedical Diagnostics (Bmd) SA, from to . As of , FDA records show no recalls naming K053383.

Clearance record

Decision date
Received
(114 days to decision)
Product code
MST Antibodies, Gliadin
Regulation
21 CFR 866.5750
Device class
Class II
Review panel
Immunology
Applicant
Biomedical Diagnostics (Bmd) SA Actipole 25, Marne La Vallee Cedex 2, FR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MST

Trailing 12 months

FDA records hold no clearances under product code MST in the trailing twelve months.

FDA records show no clearances under product code MST in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MST, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260