SONIC MANUFACTURING TECHNOLOGIES, INC.

FDA Device Registration & Listing · Fremont, CA, US · Registration 3004541594

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
3004541594
FEI Number
3004541594
Entity Name
SONIC MANUFACTURING TECHNOLOGIES, INC.
City/State/Country
Fremont, CA, US
Establishment Address
47951 WESTINGHOUSE DR, Fremont, CA 94539, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Sonic Manufacturing (Owner Number: 10051265)
Owner / Operator Contact Address
47931 Westinghouse Drive, Fremont, CA 94539, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Steris V52 RLM27HD3 The Vividimage D 27-inch HD Surgical Display Knox Medical Diagnostics A87 Aluna 2 Empo® Footprint Thimble Enso T66

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KQM Camera, Surgical And Accessories General, Plastic Surgery Class 1 878.4160 2022-02-01
BZH Meter, Peak Flow, Spirometry Anesthesiology Class 2 868.1860 2025-01-20
OIZ Foot Examination Tool For Inflammatory Changes Physical Medicine Class 1 890.5050 2025-08-05
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2022-02-03
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2022-02-03
BZH Meter, Peak Flow, Spirometry Anesthesiology Class 2 868.1860 2021-05-05

Official Correspondent

Alejandro De Leija

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sonic Manufacturing
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
K050853 Card Guard Scientific Survival , Ltd. PMP4 SPIROPRO 2005-05-04
K123945 Monaghan Medical Corp. STRIVE DUAL ZONE PEAK FLOW METER 2013-04-17
K221200 Xbody Hungary Kft. XBody Go USA, XBody Pro USA 2023-01-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004541594. Last updated year: 2026. Please use registration number 3004541594 when referencing this establishment in official correspondence.
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