Orlvision G M B H

FDA Filings

This page includes the latest FDA filings for Orlvision G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3009010438
FEI Number3009010438
NameAlla Balashov
Owner & OperatorOrlvision GmbH
Contact AddressGewerbestrasse 17
Lahnau DE-HE Hessen 35633 DE
Official Correspondent
  • Oliver Neumann
  • 49-06441-679299-0
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1244-B Quarry Lane
Pleasanton, CA 94566 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
orlvision GmbH
 Laryngoskop FS2 2020-10-27
orlvision GmbH
 Video Otoscope M-300-00000-30002020-03-16
orlvision GmbH
 Flexible Video Rhino Laryngoscope M-205-24031-01012020-03-16
orlvision GmbH
 Flexible Video Rhino Laryngoscope M-205-22031-01012020-03-16
orlvision GmbH
 Laryngoscope M2052203101012020-03-09
Alla Balashov [Orlvision GmbH]
Otoscope OX22020-03-07
Alla Balashov [Orlvision GmbH]
ORL Video Nasopharyngo-laryngoscope2019-11-05

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