Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003770530

FEI Number

3003770530

Entity Name

LEGEND AEROSPACE, INC.

City/State/Country

Miami, FL, US

Establishment Address

8292 N.W. SOUTH RIVER DR., Miami, FL 33166, US

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device

Owner / Operator

LEGEND AEROSPACE, INC. (Owner Number: 9052689)

Owner / Operator Contact Address

8292 N.W. SOUTH RIVER DR., --, Medley, FL 33166, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LAI-5532A1J LAI-5532 LAI-5532A1 LAI-5532A1-B LAI-5532A1-105 LAI-5532A1J-101 LAI-5532A1-101

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OKI	Emergency Response Safety Kit	General, Plastic Surgery	Class 2	878.4040	2008-09-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LEGEND AEROSPACE, 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 3003770530. Last updated year: 2026. Please use registration number 3003770530 when referencing this establishment in official correspondence.