CURIO DIGITAL THERAPEUTICS

FDA Device Registration & Listing · Rocky Hill, NJ, US · Registration 3036503508

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
3036503508
FEI Number
3036503508
Entity Name
CURIO DIGITAL THERAPEUTICS
City/State/Country
Rocky Hill, NJ, US
Establishment Address
10 Princeton Ave, Rocky Hill, NJ 08553, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Curio Digital Therapeutics (Owner Number: 10092756)
Owner / Operator Contact Address
10 Princeton Ave, Rocky Hill, NJ 08553, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K223515
PMA Number
N/A

All Registered Proprietary Names

MamaLift Plus

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SAP Computerized Behavioral Therapy Device For Depressive Disorders. Neurology Class 2 882.5801 2025-02-14

Official Correspondent

Indira Malladi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Curio Digital Therapeutics
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 3036503508. Last updated year: 2026. Please use registration number 3036503508 when referencing this establishment in official correspondence.
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