Data / Medical devices / United States / Path Scientific
Path Scientific: FDA-registered device maker in Carlisle, MA, United States, 1 510(k) clearance
Path Scientific is registered with the FDA (registration 3006760998) in Carlisle, MA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 31, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006760998
- Address
- Path Scientific 82 Hillside Drive, Carlisle, MA, United States, 01741
- Owner or operator
- Path Scientific (10057055)
- Roles
- Manufacturer
- First device listed
- February 15, 2018
- Registered through
- 2026
- Brand names listed
- PathFormer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Drill, Battery Powered, Subungual Hematoma | NWF | 1 | 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 |
|---|---|---|---|---|---|---|
| October 31, 2005 | K052770 | PATHFORMER | NWF | Substantially Equivalent | Path Scientific, LLC | accessdata.fda.gov |
Compare with other makers
Updated October 31, 2005. 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.