Olympus Surgical Technologies America

12 FDA 510(k) medical device clearances.

Top product codes for Olympus Surgical Technologies America

KTI — Ear, Nose, Throat 4 devices
GEX — General, Plastic Surgery 2 devices
EZN — Gastroenterology, Urology 1 device
FGE — Gastroenterology, Urology 1 device
GEI — General, Plastic Surgery 1 device
KNS — Gastroenterology, Urology 1 device
KNY — Gastroenterology, Urology 1 device
ODC — Gastroenterology, Urology 1 device

Recent clearances by Olympus Surgical Technologies America

K242191 — SOLTIVE Laser System (SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE Laser Fibers, and Accessories) GEX · 2024-08-23
K212643 — POWERSEAL Curved Jaw Sealer and Divider, Double Action GEI · 2021-09-27
K193517 — ViziShot 2 FLEX KTI · 2020-03-18
K183647 — SOLTIVE Laser System(SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVELaser Fibers, and Accessories) GEX · 2019-08-09
K190164 — CleverLock Guidewire Locking Device and Biopsy Cap ODC · 2019-04-04
K181193 — PeriView FLEX KTI · 2018-07-03
K171232 — PeriView FLEX KTI · 2017-09-21
K163469 — ViziShot 2 FLEX KTI · 2017-04-06
K143609 — Gyrus ACMI - EZDilate 3-Stage Balloon Dilatation Catheter FGE · 2015-03-27
K132181 — GYRUS ACMI URO-EZDILATE URETERAL BALLOON DILATION CATHETER EZN · 2013-10-21
K123170 — VARI-PASS VARIABLE LENGTH ACCESS SHEATH KNY · 2013-02-04
K123319 — GYRUS ACMI BICOAG HEMOSTASIS PROBE KNS · 2012-12-14

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