ADDITIVE SCALE GMBH

FDA Device Registration & Listing · Krailling Bavaria, DE · Registration 3027553893

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
3027553893
FEI Number
3027553893
Entity Name
ADDITIVE SCALE GMBH
City/State/Country
Krailling Bavaria, DE
Establishment Address
Robert-Stirling-Ring 1, Krailling Bavaria 82152, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Additive Scale GmbH (Owner Number: 10088340)
Owner / Operator Contact Address
Robert-Stirling-Ring 1, Krailling, DE-BY 82152, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Sunglasses (Non-Prescription Including Photosensitive) Frame, Spectacle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2024-06-12
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2023-06-30

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Additive Scale GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08
K852902 Yours Enterprise Co., Ltd. METALLIC SUNGLASSES 1985-08-12
K970895 Custom Optical Frames, Inc. CUSTOM OPTICAL SUNGLASS FRAMES 1997-05-06
K853921 Winsburn Company , Ltd. ALL KINDS OF SUNGLASSES 1985-10-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027553893. Last updated year: 2026. Please use registration number 3027553893 when referencing this establishment in official correspondence.
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