R2 Technologies, Inc.

FDA Device Registration & Listing · Dublin, CA, US · Registration 3025034781

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
3025034781
FEI Number
3025034781
Entity Name
R2 Technologies, Inc.
City/State/Country
Dublin, CA, US
Establishment Address
6517 Sierra Lane, Dublin, CA 94568, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
R2 Technologies, Inc. (Owner Number: 10054762)
Owner / Operator Contact Address
6517 Sierra Lane, Dublin, CA 94568, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K213294
PMA Number
N/A

All Registered Proprietary Names

Dermal Cooling System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QPZ Contact Cooling For Skin Lesion Pain Relief General, Plastic Surgery Class 2 878.4340 2022-11-17
ILO Pack, Hot Or Cold, Water Circulating Physical Medicine Class 2 890.5720 2022-11-17
GED Brush, Dermabrasion, Manual General, Plastic Surgery Class 1 878.4800 2022-11-17

Official Correspondent

Kristine Tatsutani

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

R2 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 3025034781. Last updated year: 2026. Please use registration number 3025034781 when referencing this establishment in official correspondence.
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