PLUSOPTIX GMBH

FDA Device Registration & Listing · Nuremberg Bavaria, DE · Registration 3003829667

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
3003829667
FEI Number
3003829667
Entity Name
PLUSOPTIX GMBH
City/State/Country
Nuremberg Bavaria, DE
Establishment Address
Nordostpark 21, Nuremberg Bavaria 90411, DE
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
PLUSOPTIX GMBH (Owner Number: 9050572)
Owner / Operator Contact Address
Nordostpark 21, NUERNBERG, DE-BY 90411, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

plusoptiX A12 plusoptiX A16 plusoptiX S16 plusoptiX A20 plusoptiX S20 PowerRef 3 plusoptiX S12 plusoptiX PR3

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HKO Refractometer, Ophthalmic Ophthalmic Class 1 886.1760 2002-04-04

Official Correspondent

No official correspondent registered.

US Agent Details

Christian Schmidt Business: Plusoptix Inc. Email: c.schmidt@plusoptix.com Phone: (470) 6590824

Related Public Records

Same Entity

PLUSOPTIX GMBH
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003829667. Last updated year: 2026. Please use registration number 3003829667 when referencing this establishment in official correspondence.
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