Apramed USA LLC

FDA Device Registration & Listing · Kissimmee, FL, US · Registration 3014273520

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
3014273520
FEI Number
3014273520
Entity Name
Apramed USA LLC
City/State/Country
Kissimmee, FL, US
Establishment Address
2219 CLAY ST, Kissimmee, FL 34741, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
Apramed USA LLC (Owner Number: 10056856)
Owner / Operator Contact Address
2219 Clay Street, Kissimmee, FL 34741, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Smart Chart ILLUMINIX CLARICON, CLARICON MAX, CLARICON MAX HD, CLARICON MAX Z, CLARICON MEGA, APEX INSTRUMENTS Attachment for smart phone on Slit Lamps ORBIT X, ORBIT Essence / Apex Instruments EagleSight RefraScan ORBIT, ORBIT X

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2018-01-25
PUE Biomicroscope, Slit-Lamp, Ac-Powered, Exempt Ophthalmic Class 2 886.1850 2018-04-23
HMF Stand, Instrument, Ac-Powered, Ophthalmic Ophthalmic Class 1 886.1860 2018-01-23
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2018-08-31
HKO Refractometer, Ophthalmic Ophthalmic Class 1 886.1760 2024-01-19
NOI Stand, Instrument, Ophthalmic, Battery Powered Ophthalmic Class 1 886.1860 2018-01-23

Official Correspondent

Justin Robertson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Apramed USA LLC
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 3014273520. Last updated year: 2026. Please use registration number 3014273520 when referencing this establishment in official correspondence.
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