510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K210006Substantially Equivalent

MI DeTACH

Biorep Technologies, Inc., Miami Lakes FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K210006 is the FDA 510(k) clearance record for MI DeTACH, a class II device, cleared for Biorep Technologies, Inc. on under FDA product code DXC (Clamp, Vascular). FDA records list one 510(k) clearance for Biorep Technologies, Inc. As of , FDA records show no recalls naming K210006.

Clearance record

Decision date
Received
(59 days to decision)
Product code
DXC Clamp, Vascular
Regulation
21 CFR 870.4450
Device class
Class II
Review panel
Cardiovascular
Applicant
Biorep Technologies, Inc. 15804 NW 57th Ave., Miami Lakes FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DXC

Trailing 12 months
6 clearances under product code DXC in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXC, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20261
May 20261
June 20261
July 20261
August 20260
September 20260
October 20260