RAPID RELEASE TECHNOLOGIES

FDA Device Registration & Listing · Costa Mesa, CA, US · Registration 3009341046

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
3009341046
FEI Number
3009341046
Entity Name
RAPID RELEASE TECHNOLOGIES
City/State/Country
Costa Mesa, CA, US
Establishment Address
3303 Harbor Blvd, Suite D-10, Costa Mesa, CA 92626, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Rapid Release Technologies (Owner Number: 10038106)
Owner / Operator Contact Address
3303 Harbor Blvd, Suite D-10, Costa Mesa, CA 92626, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Rapid Release Pro3

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IRO Vibrator, Therapeutic Physical Medicine Class 1 890.5975 2011-09-15

Official Correspondent

Jeff Maier

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Rapid Release Technologies
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K821133 Durham Electric Co. ELECTRICAL VIBRATING DEVICE 1982-07-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009341046. Last updated year: 2026. Please use registration number 3009341046 when referencing this establishment in official correspondence.
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