ROM Technologies, Inc.

FDA Device Registration & Listing · Brookfield, CT, US · Registration 3015060244

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
3015060244
FEI Number
3015060244
Entity Name
ROM Technologies, Inc.
City/State/Country
Brookfield, CT, US
Establishment Address
101 Silvermine Rd, Brookfield, CT 06804, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ROM Technologies, Inc (Owner Number: 10058435)
Owner / Operator Contact Address
101 Silvermine Rd, Brookfield, CT 06804, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PortableConnect Rehab System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKK System, Isokinetic Testing And Evaluation Physical Medicine Class 2 890.1925 2018-10-03

Official Correspondent

Christian Svejk

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ROM Technologies, 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 3015060244. Last updated year: 2026. Please use registration number 3015060244 when referencing this establishment in official correspondence.
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