PATH SCIENTIFIC

FDA Device Registration & Listing · Carlisle, MA, US · Registration 3006760998

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3006760998
FEI Number
3006760998
Entity Name
PATH SCIENTIFIC
City/State/Country
Carlisle, MA, US
Establishment Address
Path Scientific, 82 Hillside Drive, Carlisle, MA 01741, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Path Scientific (Owner Number: 10057055)
Owner / Operator Contact Address
Path Scientific, 82 Hillside Drive, Carlisle, MA 01741, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K052770
PMA Number
N/A

All Registered Proprietary Names

PathFormer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NWF Drill, Battery Powered, Subungual Hematoma General, Plastic Surgery Class 1 878.4820 2018-02-15

Official Correspondent

Patsy Trisler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Path Scientific
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006760998. Last updated year: 2026. Please use registration number 3006760998 when referencing this establishment in official correspondence.
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