HYPERICE, INC.

FDA Device Registration & Listing · Irvine, CA, US · Registration 3010008676

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
3010008676
FEI Number
3010008676
Entity Name
HYPERICE, INC.
City/State/Country
Irvine, CA, US
Establishment Address
525 Technology Drive, Suite 100, Irvine, CA 92618, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Hyperice, Inc. (Owner Number: 10049409)
Owner / Operator Contact Address
525 Technology Drive, Suite 100, Irvine, CA 92618, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Heated Head Venom 2 Back Venom Shoulder Venom GO Venom Leg Venom 2 Leg Venom 2 Shoulder Venom Venom Shoulder Hypervolt Venom Leg Venom Raptor Vyper Hypersphere Hypervolt BT Hypervolt 2 Hypervolt 2 Pro Vyper Go Hypervolt GO Vyper 3 Hypervolt Go 2 Venom 2 Back Venom 2 Shoulder Venom 2 Leg Hypersphere Mini Venom GO Hypervolt 3 Pro Hypervolt 3 Hypersphere Go Hypervolt Go 3

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IRT Pad, Heating, Powered Physical Medicine Class 2 890.5740 2023-11-16
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2017-12-18

Official Correspondent

Steve Henderson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hyperice, Inc.
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
K881862 Thermo Body Wrap Systems, Inc. THERMO-BODY-WRAP SYSTEM 1988-10-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010008676. Last updated year: 2026. Please use registration number 3010008676 when referencing this establishment in official correspondence.
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