510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K033210Substantially Equivalent

Bioteq Double Pigtail Ureteral Stent Set

Bioteque Corp., Flagstaff AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K033210 is the FDA 510(k) clearance record for BIOTEQ DOUBLE PIGTAIL URETERAL STENT SET, a class II device, cleared for Bioteque Corp. on under FDA product code FAD (Stent, Ureteral). FDA records list 14 510(k) clearances for Bioteque Corp., from to . As of , FDA records show no recalls naming K033210.

Clearance record

Decision date
Received
(454 days to decision)
Product code
FAD Stent, Ureteral
Regulation
21 CFR 876.4620
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Bioteque Corp. 3892 S. America W. Trl., Flagstaff AZ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FAD

Trailing 12 months
2 clearances under product code FAD in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FAD, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260