Monday, October 26, 2026 · Daily editionET --:--:--

MedicalMicrosurgery robot

Symani

by MMI (Medical Microinstruments)

Symani is a surgical robot for microsurgery: stitching together blood and lymph vessels thinner than a millimetre. It scales down the surgeon's hand movements and filters out hand tremor. MassDevice, 8 Apr 2024

5

Stage 5 of 5

Regulator-cleared or mass market

Which rule placed it
Evidence
Independently reported
Human help
None reported
Last milestone
4 May 2026

01Can I get it?

Yes, in places

Where it works today
Used in hospitals in Europe, and in the US since 2024 (first US cases at Penn Presbyterian Medical Center). MassDevice, 1 May 2024
Published price
No published price in our sources.
Human help
A surgeon controls the robot from a console; the robot scales down and steadies the movements.

03Safety and incidents

What has gone wrong

No crashes, recalls or regulator reports in our sources. That is not proof none happened; we add them when a regulator or trusted outlet reports one.

How we placed it

The rule, not an opinion

Stages are worked out by published rules from the dated milestones above. We never rate robots, and no maker can pay to change a stage.

  1. 5

    Regulator-cleared or mass marketThis robot

    A regulator has cleared it where approval applies: FDA clearance or approval for a medical robot, a permit to run with no one aboard for a self-driving vehicle, or an FAA approval for routine drone flights. Or: Widely sold: sales in the hundreds of thousands, or a product category you can buy in ordinary shops.

    Placed by: The FDA cleared Symani through the De Novo route (DEN230032) for microsurgery on soft tissue (5 April 2024).

  2. 4

    Paying customers

    Delivered to customers who pay for it, beyond a trial, or a paid service the public can use.

  3. 3

    Pilot

    Working with a named customer in a real setting, as a trial.

  4. 2

    Pre-orders

    Orders, reservations or deposits taken, with nothing delivered yet.

  5. 1

    Demo only

    Shown in videos, staged events or a factory, with no units working for customers.

What we couldn't confirm. MassDevice gives conflicting CE mark dates (2019 in a 2024 article; a 2020 headline), so the European approval is left out. No recall check or funding figures due to a research tool limit. The Alzheimer's use is experimental, under an FDA study exemption.