510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071210Substantially Equivalent

Modification to Fidis Connective 10*, Model Mx006

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)

K071210 is the FDA 510(k) clearance record for MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006, a class II device, cleared for Biomedical Diagnostics (Bmd) SA on under FDA product code LKO (Anti-Rnp Antibody, Antigen And Control). FDA records list 10 510(k) clearances for Biomedical Diagnostics (Bmd) SA, from to . As of , FDA records show no recalls naming K071210.

Clearance record

Decision date
Received
(232 days to decision)
Product code
LKO Anti-Rnp Antibody, Antigen And Control
Regulation
21 CFR 866.5100
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 LKO

Trailing 12 months

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

FDA records show no clearances under product code LKO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LKO, 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