SCHOELLY FIBEROPTIC, GMBH

FDA Device Registration & Listing · DENZLINGEN Baden-Wurttemberg, DE · Registration 8043903

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
8043903
FEI Number
3002808088
Entity Name
SCHOELLY FIBEROPTIC, GMBH
City/State/Country
DENZLINGEN Baden-Wurttemberg, DE
Establishment Address
ROBERT-BOSCH-STR. 1-3, DENZLINGEN Baden-Wurttemberg 79211, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SCHOELLY FIBEROPTIC, GMBH (Owner Number: 9004385)
Owner / Operator Contact Address
ROBERT-BOSCH-STR. 1-3, --, DENZLINGEN, DE-NOTA 79211, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Arthroscopes Uretero-Renoscope Sealing caps Three slot membrane Light guides Hysteroscopes Cystoscopes Laparoscopes Endoscopic Camera Control Unit NIR FI Light Source Endoscopic Camera Heads 2D NIR FI Laparoscopes

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HRX Arthroscope Orthopedic Class 2 888.1100 2014-10-15
NAY System, Surgical, Computer Controlled Instrument Gastroenterology, Urology Class 2 876.1500 2013-03-08
GCJ Laparoscope, General & Plastic Surgery Gastroenterology, Urology Class 2 876.1500 2025-08-08
FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology Gastroenterology, Urology Class 2 876.1500 2021-03-18
GCJ Laparoscope, General & Plastic Surgery Gastroenterology, Urology Class 2 876.1500 2021-03-18
HET Laparoscope, Gynecologic (And Accessories) Obstetrics/Gynecology Class 2 884.1720 2021-03-18
FGB Ureteroscope And Accessories, Flexible/Rigid Gastroenterology, Urology Class 2 876.1500 2008-03-10
EQH Source, Carrier, Fiberoptic Light Ear, Nose, Throat Class 1 874.4350 2011-01-27
GCJ Laparoscope, General & Plastic Surgery Gastroenterology, Urology Class 2 876.1500 2024-09-09
FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology Gastroenterology, Urology Class 2 876.1500 2024-09-09
EOB Nasopharyngoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4760 2015-11-10
CCW Laryngoscope, Rigid Anesthesiology Class 1 868.5540 2011-08-08
EOB Nasopharyngoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4760 2022-04-06
NAY System, Surgical, Computer Controlled Instrument Gastroenterology, Urology Class 2 876.1500 2013-03-08
FAJ Cystoscope And Accessories, Flexible/Rigid Gastroenterology, Urology Class 2 876.1500 2015-03-12
HIH Hysteroscope (And Accessories) Obstetrics/Gynecology Class 2 884.1690 2015-03-12
GCJ Laparoscope, General & Plastic Surgery Gastroenterology, Urology Class 2 876.1500 2015-01-29
OWN Confocal Optical Imaging Gastroenterology, Urology Class 2 876.1500 2023-06-06
GCJ Laparoscope, General & Plastic Surgery Gastroenterology, Urology Class 2 876.1500 2023-06-06
FCW Light Source, Fiberoptic, Routine Gastroenterology, Urology Class 2 876.1500 2023-06-06
FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology Gastroenterology, Urology Class 2 876.1500 2023-06-06
FGA Kit, Nephroscope Gastroenterology, Urology Class 2 876.1500 2016-02-11
FED Endoscopic Access Overtube, Gastroenterology-Urology Gastroenterology, Urology Class 2 876.1500 2016-02-11
FEC Obturator, For Endoscope Gastroenterology, Urology Class 2 876.1500 2016-02-11
EOB Nasopharyngoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4760 2009-10-20

Official Correspondent

GERHARD HERBSTRITT

US Agent Details

James Bonneville Business: SCHOELLY USA Inc. Email: j.bonneville@schoelly-usa.com Phone: (508) 9268855

Related Public Records

Same Entity

SCHOELLY FIBEROPTIC, GMBH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3014644276 SCHOELLY-OPTIX OOD Panagyurishte Pazardzhik, BG

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K081051 Spine View, Inc. SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS), SPINEVU MINISCOPE 2008-08-07
K820777 The Anspach Effort, Inc. MINI-MICRO ARTHROSCOPIC SCAPEL 1982-05-12
K914997 Conmedcorp ASP-IRRATOR 1992-01-07
K153773 Olympus Medical Systems Corp. Disposal Lens Cleaning Sheath 2016-11-22
K940141 Micro-Medical Devices, Inc. LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH 1994-05-19

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0041-05 Linvatec Corp. 2
Ultra Power Burs, Sterile, Single-Use.
Z-0027-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Lap Banding Kit, REF: K0398 Contains: (2) C0Q04, 5x100mm Threaded Kii Access System (1) C0604, 15x100mm Non-Threaded Separator System w/Universal Seal, for laparoscopic procedures.
Z-0028-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Lap Banding Kit, REF: K0406 Contains: (1) C0658, 11x100mm Threaded Shielded Trocar w/Universal Seal (1) C0522, 5x100mm Threaded Premium Flat Blade (1) C2202, 150mm Insufflation needle (1) C0605, 15x100mm Threaded Separator Access System (1) CB030, 5mm x 35cm Direct Drive Disposable Scissors (2) C4120, 5mm x 38cm Direct Drive Grasper Reposable Cartridge, for laparoscopic procedures.
Z-0029-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Lap Roux-EN-Y Kit, REF: K2129 Contains: (1) C0Q04, 5x100mm Threaded Kii Access System (1) C0130, 12x100mm Optical Separator System, Non-handled (2) C0Q10, 5x100mm Threaded Kii Cannula and Seal (1) C0605, 15mmx100mm Threaded Cannula System, for laparoscopic procedures.
Z-0023-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Separator Abdominal Access System REF: C0604 15 x 100mm Non-threaded Separator System with Universal Seal, for laparoscopic procedures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8043903. Last updated year: 2026. Please use registration number 8043903 when referencing this establishment in official correspondence.
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