Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011209824

FEI Number

3011209824

Entity Name

ActivArmor

City/State/Country

Port Saint Lucie, FL, US

Establishment Address

6776 NW Cloverdale Ave, Port Saint Lucie, FL 34987, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

ActivArmor (Owner Number: 10047482)

Owner / Operator Contact Address

6776 NW Cloverdale Ave, Port Saint Lucie, FL 34987, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ActivArmor Casts and Splints

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NOC	Splint, Extremity, Non-Inflatable, External, Non-Sterile	General, Plastic Surgery	Class 1	878.3910	2014-09-16

Official Correspondent

Diana Hall

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ActivArmor

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 3011209824. Last updated year: 2026. Please use registration number 3011209824 when referencing this establishment in official correspondence.