Data / Medical devices / Italy / Medical Microinstruments, Inc.
Medical Microinstruments, Inc.: FDA-registered device maker in Pisa, Italy, 5 510(k) clearances
Medical Microinstruments, Inc. is registered with the FDA (registration 3030831003) in Pisa, Italy. It lists 1 device type. The FDA files 5 510(k) clearances under its listings, the newest dated November 10, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030831003
- Address
- Via Egidio Giannessi 54, Pisa, Italy, 56121
- Owner or operator
- Medical Microinstruments, Inc. (10090513)
- Roles
- Manufacturer
- First device listed
- April 7, 2024
- Registered through
- 2026
- Brand names listed
- Symani Surgical System, Symani® Surgical System, Symani® Surgical System - Forceps and Scissors Instruments, Symani® Surgical System - Supermicro Needle Holeder Suture Cut
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electromechanical System For Open Microsurgery | SAQ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 10, 2025 | K252287 | Symani Surgical System | SAQ | Substantially Equivalent | Medical Microinstruments, Inc. | accessdata.fda.gov |
| September 4, 2025 | K251510 | Symani Surgical System | SAQ | Substantially Equivalent | Medical Microinstruments, Inc. | accessdata.fda.gov |
| February 7, 2025 | K242368 | Symani Surgical System | SAQ | Substantially Equivalent | Medical Microinstruments, Inc. | accessdata.fda.gov |
| January 27, 2025 | K250014 | Symani Surgical System (820-03830) | SAQ | Substantially Equivalent | Medical Microinstruments, Inc. | accessdata.fda.gov |
| April 5, 2024 | DEN230032 | Symani Surgical System | SAQ | Unknown | Mmi North America, Inc. | accessdata.fda.gov |
Updated November 10, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.