Boyd Corporation GmbH

FDA Device Registration & Listing · Syke Lower Saxony, DE · Registration 3012866928

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
3012866928
FEI Number
3012866928
Entity Name
Boyd Corporation GmbH
City/State/Country
Syke Lower Saxony, DE
Establishment Address
Rudolf-Diesel Strasse 17, Syke Lower Saxony 28857, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Boyd Corporation GmbH (Owner Number: 10052843)
Owner / Operator Contact Address
Rudolf-Diesel Strasse 17, Syke, DE-NI 28857, DE
Initial Importer Flag
N
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
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2023-09-19
DPZ Oximeter, Ear Cardiovascular Class 2 870.2710 2016-10-11
KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia Anesthesiology Class 2 868.2500 2016-10-11
LPP Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia Anesthesiology Class 2 868.2500 2016-10-11
LKD Monitor, Carbon-Dioxide, Cutaneous Anesthesiology Class 2 868.2480 2016-10-11

Official Correspondent

Ortwin Segelhorst

US Agent Details

Stephen Gorski Business: Imagenix, Inc. Email: stephengorski@me.com Phone: (414) 7374596

Related Public Records

Same Entity

Boyd Corporation 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
K893133 Mennen Medical, Inc. HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX 1989-07-14

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012866928. Last updated year: 2026. Please use registration number 3012866928 when referencing this establishment in official correspondence.
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