Silgan Dispensing Systems Hemer GmbH

FDA Device Registration & Listing · HEMER North Rhine-Westphalia, DE · Registration 8010692

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
8010692
FEI Number
3007056352
Entity Name
Silgan Dispensing Systems Hemer GmbH
City/State/Country
HEMER North Rhine-Westphalia, DE
Establishment Address
Ernst-Stenner Strasse 17, HEMER North Rhine-Westphalia 58675, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Silgan Dispensing Systems Germany GmbH (Owner Number: 8010692)
Owner / Operator Contact Address
Ernst-Stenner-Strasse 17, --, Hemer, DE-NOTA 58675, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Iridya Eye Dropper

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2019-11-28

Official Correspondent

No official correspondent registered.

US Agent Details

Connelia Savage Business: Vice President, General Counsel, Regulatory & Sustainability Email: Connelia.Savage@silgandispensing.com Phone: (804) 6299886

Related Public Records

Same Entity

Silgan Dispensing Systems Germany 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 8010692. Last updated year: 2026. Please use registration number 8010692 when referencing this establishment in official correspondence.
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