SCHOTT NORTH AMERICA INC - LIGHTING AND IMAGING

FDA Device Registration & Listing · Southbridge, MA, US · Registration 3009162689

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
3009162689
FEI Number
3009162689
Entity Name
SCHOTT NORTH AMERICA INC - LIGHTING AND IMAGING
City/State/Country
Southbridge, MA, US
Establishment Address
122 Charlton St, Southbridge, MA 01550, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
SCHOTT North America Inc - Lighting and Imaging (Owner Number: 10036067)
Owner / Operator Contact Address
122 Charlton Street, Southbridge, MA 01550, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EQH Source, Carrier, Fiberoptic Light Ear, Nose, Throat Class 1 874.4350 2011-04-18

Official Correspondent

Joshua Beu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SCHOTT North America Inc - Lighting and Imaging
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 3009162689. Last updated year: 2026. Please use registration number 3009162689 when referencing this establishment in official correspondence.
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