KARL KAPS GMBH & CO. KG

FDA Device Registration & Listing · ASSLAR Hesse, DE · Registration 9610810

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
9610810
FEI Number
3002807375
Entity Name
KARL KAPS GMBH & CO. KG
City/State/Country
ASSLAR Hesse, DE
Establishment Address
EUROPASTRASSE, ASSLAR Hesse D-35614, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KARL KAPS GMBH & CO. KG (Owner Number: 8010499)
Owner / Operator Contact Address
EUROPASTRASSE, --, ASSLAR, DE-NOTA D-35614, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

KAPS OPERATING MICROS STANDARD LABORATORY OPERATING MICROSCOPE SOM I

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EPT Microscope, Surgical General, Plastic Surgery Class 1 878.4700 1979-03-01
HRM Microscope, Operating & Accessories, Ac-Powered, Ophthalmic General, Plastic Surgery Class 1 878.4700 1979-03-01

Official Correspondent

HOLGER KAPS

US Agent Details

Dustin Biggerstaff Business: JEDMED Email: dustinb@JEDMED.com Phone: (314) 8453770

Related Public Records

Same Entity

KARL KAPS GMBH & CO. KG
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 9610810. Last updated year: 2026. Please use registration number 9610810 when referencing this establishment in official correspondence.
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