Data / Medical devices / United States / Parallel Robotics, LLC
Parallel Robotics, LLC: FDA-registered device maker in Ann Arbor, MI, United States, 1 510(k) clearance
Parallel Robotics, LLC is registered with the FDA (registration 3048176670) in Ann Arbor, MI, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 24, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3048176670
- Address
- 3810 Packard St Ste 100a, Ann Arbor, MI, United States, 48108
- Owner or operator
- Parallel Robotics (10096233)
- Roles
- Manufacturer
- First device listed
- July 31, 2026
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Laparoscope, General & Plastic Surgery | GCJ | 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 |
|---|---|---|---|---|---|---|
| May 24, 2026 | K260183 | MediBot Needle Driver Uno | GCJ | Substantially Equivalent | Parallel Robotics, LLC | accessdata.fda.gov |
Compare with other makers
Updated May 24, 2026. 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.