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Data / Medical devices / Germany / Oberon GMBH Fiber Technologies

Oberon GMBH Fiber Technologies: FDA-registered device maker in Wildau Brandenburg, Germany, 1 510(k) clearance

Oberon GMBH Fiber Technologies is registered with the FDA (registration 3011310540) in Wildau Brandenburg, Germany. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 15, 2014. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3011310540
Address
Ludwig-Witthoeft-Strasse 14, Wildau Brandenburg, Germany, 15745
Owner or operator
OBERON GmbH Fiber Technologies (10047817)
Roles
Manufacturer
First device listed
November 4, 2014
Registered through
2026
Brand names listed
Side Fire Fibers, Surgical Laser Fibers, Vascular Laser Fibers

Devices it lists

DeviceProduct codeClassRoleSource
Powered Laser Surgical InstrumentGEX2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
October 15, 2014K140470OBERON: LASER SURGERY FIBER, ATRAUMATIC SURGERY FIBER, SIDE FIRE FIBER, RADIAL EMISSION FIBER, DENTAL SURGERY FIBERGEXSubstantially EquivalentOberon GmbH Fiber Technologiesaccessdata.fda.gov

Compare with other makers

Updated October 15, 2014. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.