Symani Surgical System— 510(k) DEN230032

Unknown

Mmi North America, Inc.

FDA 510(k) clearance DEN230032 for Symani Surgical System, Unknown on 2024-04-05. Applicant: Mmi North America, Inc.. Device class: 2.

Clearance details

Applicant: Mmi North America, Inc.
Product code: Code SAQ
Device class: Class 2
Regulation: 21 CFR 878.4963
Advisory panel: General, Plastic Surgery
Date received: 2023-04-25
Decision date: 2024-04-05
Decision: Unknown
Clearance type: Direct
Location: Ponte Vedra, FL, US

View on FDA.gov ↗

Recent devices under product code SAQ

K252287 — Symani Surgical System2025-11-10
K251510 — Symani Surgical System2025-09-04
K242368 — Symani Surgical System2025-02-07
K250014 — Symani Surgical System (820-03830)2025-01-27

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