VERIDIAM

FDA Device Registration & Listing · Oceanside, CA, US · Registration 3007284295

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
3007284295
FEI Number
1000306517
Entity Name
VERIDIAM
City/State/Country
Oceanside, CA, US
Establishment Address
4665 North Ave, Oceanside, CA 92056, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Veridiam, Inc (Owner Number: 10046309)
Owner / Operator Contact Address
1717 North Cuyamaca Street, El Cajon, CA 92020, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ADJUSTABLE TORQUE WRENCH (ATR) Universal Drill Extender

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HXC Wrench Orthopedic Class 1 888.4540 2017-12-29
DZA Drill, Dental, Intraoral Dental Class 1 872.4130 2017-12-29

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Veridiam, Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3009161688 VERIDIAM, INC El Cajon, CA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007284295. Last updated year: 2026. Please use registration number 3007284295 when referencing this establishment in official correspondence.
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