Olympus Surgical Technologies America
Olympus Surgical Technologies America holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2026.
Top product codes for Olympus Surgical Technologies America
Recent clearances by Olympus Surgical Technologies America
- K261221 — SOLTIVE Laser System (SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE Laser Fibers, and Accessories)
- K242191 — SOLTIVE Laser System (SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE Laser Fibers, and Accessories)
- K212643 — POWERSEAL Curved Jaw Sealer and Divider, Double Action
- K193517 — ViziShot 2 FLEX
- K183647 — SOLTIVE Laser System(SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVELaser Fibers, and Accessories)
- K190164 — CleverLock Guidewire Locking Device and Biopsy Cap
- K181193 — PeriView FLEX
- K171232 — PeriView FLEX
- K163469 — ViziShot 2 FLEX
- K143609 — Gyrus ACMI - EZDilate 3-Stage Balloon Dilatation Catheter
- K132181 — GYRUS ACMI URO-EZDILATE URETERAL BALLOON DILATION CATHETER
- K123170 — VARI-PASS VARIABLE LENGTH ACCESS SHEATH
- K123319 — GYRUS ACMI BICOAG HEMOSTASIS PROBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.