Aprios Custom MFG

FDA Device Registration & Listing · Vista, CA, US · Registration 3014552222

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
3014552222
FEI Number
3014552222
Entity Name
Aprios Custom MFG
City/State/Country
Vista, CA, US
Establishment Address
1333 Keystone Way, Vista, CA 92081, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
PACIFIC PLASTICS INJECTION MOLDING (Owner Number: 10088301)
Owner / Operator Contact Address
1333 Keystone Way, Vista, CA 92081, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PLV Dental Stereotaxic Instrument Dental Class 2 872.4120 2023-06-26
QRY Dental Navigation System Dental Class 2 872.4120 2023-06-26

Official Correspondent

PABLO SOTO

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PACIFIC PLASTICS INJECTION MOLDING
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014552222. Last updated year: 2026. Please use registration number 3014552222 when referencing this establishment in official correspondence.
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