Data / Medical devices / United States / Medusa Orthopedics, LLC
Medusa Orthopedics, LLC: FDA-registered device maker in Fleetwood, PA, United States, 1 510(k) clearance
Medusa Orthopedics, LLC is registered with the FDA (registration 3044090645) in Fleetwood, PA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 25, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3044090645
- Address
- 190 S View rd, Fleetwood, PA, United States, 19522
- Owner or operator
- Medusa Orthopedics, LLC (10095445)
- Roles
- Manufacturer
- First device listed
- March 13, 2026
- Registered through
- 2026
- Brand names listed
- Medusa Orthopedics Boa External Fixation System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component | KTT | 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 25, 2025 | K252555 | Medusa Orthopedics Boa External Fixation System | KTT | Substantially Equivalent | Medusa Orthopedics, LLC | accessdata.fda.gov |
Compare with other makers
Updated November 25, 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.