Orsense

FDA Filings

This page includes the latest FDA filings for Orsense. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3007358963
FEI Number3007358963
NameCharles Neff
Owner & OperatorOrSense
Contact Address17 HaMefalsim St., Kiryat Arie POB 10383
Petah-Tikva IL-M HaMerkaz 4900302 IL
Official Correspondent
  • Aharon Weinstein
  • 972-3-7404901-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address10900 world trade blvd , suite:205
Raleigh, NC 27617 US
Establishment TypeManufacture Medical Device

FDA Owner/Operator Registration

FDA Filings

Device
Company
DeviceDate
Charles Neff [OrSense]
NBM-200 Pulse Oximeter and Hemoglobin Monitor2019-06-18
Charles Neff [OrSense]
NBM-200 Pulse Oximeter2015-01-18
Charles Neff [OrSense]
NBM-200 Pulse Oximeter and Hemoglobin Monitor2015-01-18
Charles Neff [OrSense]
NBM-200 Pulse Oximeter2015-01-18
Charles Neff [OrSense]
NBM-200 Pulse Oximeter and Hemoglobin Monitor2015-01-18
Charles Neff [OrSense]
NBM-200MP Pulse Oximeter2014-02-16
Charles Neff [OrSense]
NBM-200MP Pulse Oximeter and Hemoglobin Monitor2014-02-16
Charles Neff [OrSense]
NBM-200MP Pulse Oximeter2014-02-16
Charles Neff [OrSense]
NBM-200MP Pulse Oximeter and Hemoglobin Monitor2014-02-16
Charles Neff [OrSense]
NBM-200MP Pulse Oximeter2010-05-04

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