Surgitech, Inc.

FDA Device Registration & Listing · Carlsbad, CA, US · Registration 2032724

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
2032724
FEI Number
3004014634
Entity Name
Surgitech, Inc.
City/State/Country
Carlsbad, CA, US
Establishment Address
2772 Gateway Rd, Carlsbad, CA 92009, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Surgitech, Inc. (Owner Number: 10023623)
Owner / Operator Contact Address
2772 Gateway Road, Carlsbad, CA 92009, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Chronic Pain Suppressor CPS-2000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LIH Interferential Current Therapy Neurology Class 2 882.5890 2007-12-05

Official Correspondent

Christopher Crowell

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Surgitech, Inc.
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 2032724. Last updated year: 2026. Please use registration number 2032724 when referencing this establishment in official correspondence.
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