SENSE TECHNOLOGY, INC.

FDA Device Registration & Listing · Halifax, PA, US · Registration 2530787

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
2530787
FEI Number
1000522110
Entity Name
SENSE TECHNOLOGY, INC.
City/State/Country
Halifax, PA, US
Establishment Address
1033 Matamoras RD, Halifax, PA 17032, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
SENSE TECHNOLOGY, INC. (Owner Number: 9012406)
Owner / Operator Contact Address
1033 Matamoras RD, Halifax, PA 17032, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K973914
PMA Number
N/A

All Registered Proprietary Names

PulStarFRAS FRAS PulStar ProAdjuster Vision PrecisionM5

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXM Manipulator, Plunger-Like Joint Unknown Class U N/A 2007-12-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SENSE TECHNOLOGY, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2530787. Last updated year: 2026. Please use registration number 2530787 when referencing this establishment in official correspondence.
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