VITAFORM, INC.

FDA Device Registration & Listing · Dana Point, CA, US · Registration 3015426612

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
3015426612
FEI Number
3015426612
Entity Name
VITAFORM, INC.
City/State/Country
Dana Point, CA, US
Establishment Address
34145 Pacific Coast Hwy, Suite 311, Dana Point, CA 92629, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device
Owner / Operator
Vitaform, Inc. (Owner Number: 10060051)
Owner / Operator Contact Address
34145 Pacific Coast Hwy, Suite 311, Dana Point, CA 92629, US
Initial Importer Flag
Y
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
MDR Binder, Medical, Therapeutic General Hospital Class 1 880.5160 2019-03-28
ITW Joint, Ankle, External Brace Physical Medicine Class 1 890.3475 2023-09-21
IQE Orthosis, Lumbar Physical Medicine Class 1 890.3490 2024-04-04

Official Correspondent

Don Francisco

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vitaform, Inc.
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 3015426612. Last updated year: 2026. Please use registration number 3015426612 when referencing this establishment in official correspondence.
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