510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K033188Substantially Equivalent

Texan Foreign Body Retrieval Device, Model Tx30060050

Idev Technologies, Inc., Houston TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K033188 is the FDA 510(k) clearance record for TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050, a class II device, cleared for Idev Technologies, Inc. on under FDA product code MMX (Device, Percutaneous Retrieval). FDA records list 11 510(k) clearances for Idev Technologies, Inc., from to . As of , FDA records show no recalls naming K033188.

Clearance record

Decision date
Received
(49 days to decision)
Product code
MMX Device, Percutaneous Retrieval
Regulation
21 CFR 870.5150
Device class
Class II
Review panel
Cardiovascular
Applicant
Idev Technologies, Inc. 1110 Nasa Rd., Suite 311, Houston TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MMX

Trailing 12 months

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

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