APARATA MEDICAL

FDA Device Registration & Listing · Orlando, FL, US · Registration 3030979378

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
3030979378
FEI Number
3030979378
Entity Name
APARATA MEDICAL
City/State/Country
Orlando, FL, US
Establishment Address
1126 S Division Ave, Orlando, FL 32805, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Aparata Medical (Owner Number: 10090523)
Owner / Operator Contact Address
1414 Kuhl Ave., Orlando, FL 32806, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bleed ID Suction Pad SafeSplint - Short Arm Splint

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered General Hospital Class 2 880.6740 2026-02-23
FZF Splint, Extremity, Inflatable, External General, Plastic Surgery Class 1 878.3900 2024-04-08

Official Correspondent

Riham Hanna

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aparata Medical
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 3030979378. Last updated year: 2026. Please use registration number 3030979378 when referencing this establishment in official correspondence.
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