Aragon Surgical, Inc.

Aragon Surgical, Inc. holds 6 FDA 510(k) medical device clearances, first cleared 2007, most recent 2011.

Top product codes for Aragon Surgical, Inc.

GEI — General, Plastic Surgery4 devices
HIF — Obstetrics/Gynecology2 devices

Recent clearances by Aragon Surgical, Inc.

K110824 — ARAGON SURGICAL RF SYSTEM - 5MM LAPAROSCOPIC INSTRUMENTCode GEI·2011-07-11
K093075 — ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENTCode GEI·2010-01-21
K090306 — ARAGON SURGICAL RF SYSTEM L2 INSTRUMENTCode GEI·2009-06-18
K081312 — ARAGON ONESHOT SYSTEMCode GEI·2008-10-31
K073452 — MODIFICATION TO: ARAGON SURGICAL LAPCAPCode HIF·2008-01-11
K070651 — ARAGON SURGICAL LAPCAPCode HIF·2007-05-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.