Product code FEO— Gastroenterology, Urology
Swiss LithoClast Trilogy
- Classification name
- Lithotriptor, Ultrasonic
- Device class
- Class 2
- Regulation
- 21 CFR 876.4480
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 14
- First cleared
- Most recent
Market context for product code FEO
FDA has cleared devices under product code FEO between 1984 and 2023, filed by 7 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2023
- 2018
- 2017
- 2014
- 1999
- 1998
- 1992
- 1987
- 1985
- 1984
Top applicants under product code FEO
Adverse events under product code FEO
product code FEO- Malfunction
- 910
- Other
- 1
- Total
- 911
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code FEO
- K230893 — Swiss LthoClast Trilogy
- K182490 — Swiss LithoClast Trilogy
- K181997 — Swiss LithoClast Trilogy
- K181364 — Swiss LithoClast Trilogy
- K173234 — Swiss LithoClast Trilogy
- K171024 — ShockPulse-SE Lithotripsy System
- K142428 — Shock Pulse-SE Lithotripsy System CYBERWAND II
- K993046 — FIBRA SONICS ULTRASONIC LITHOTRIPTOR LITHOSONIC, MODEL LS-2000
- K973251 — KSEA CALCUSON
- K920235 — ULTRASOUND GENERATOR MODLE 2270
- K873367 — OLYMPUS LUS ULTRASONIC LITHOTRIPTER
- K850298 — ULTRALITH ULTRASONIC LITHOTRIPSY SYSTEM
- K842024 — ULTRASONIC LITHOTRIPTOR 300A
- K843101 — KARL STORZ 27086KC ULTRASONIC LITHOTRI
Data sourced from openFDA. This site is unofficial and independent of the FDA.