FDA Registration Active 🇺🇸 United States

Verathon Inc.

Reg #: 3022472 · FEI: 3022472 · Expires 2026
Products
6
Proprietary Names
15
Establishment Types
2
Classifications
6

Registration Details

Registration Name
Verathon Inc.
Registration Number
3022472
FEI Number
3022472
Status
Active
Expiry Year
2026
Initial Importer
Yes
Address
20001 North Creek Pkwy
City
BOTHELL
State
WA
ZIP
98011
Country
US

Regulatory Submissions

510(k) Number
K153101

Owner / Operator

Firm Name
Verathon Inc.
Operator Number
3022472
Address
20001 North Creek Pkwy
City
Bothell
State
WA
Postal Code
98011
Country
US
Correspondent
Jonathan Stevens

Products

Device Name Product Code
System, Imaging, Pulsed Echo, Ultrasonic IYO
Transducer, Ultrasonic, Diagnostic ITX
Bronchoscope (Flexible Or Rigid) EOQ
Laryngoscope, Rigid CCW
Stylet, Tracheal Tube BSR
Uroflowmeter EXY

Proprietary Names

BladderScan® Prime GlideScope® BFlex™ 2.8 Single-Use Bronchoscope System GlideScope® BFlex™ 3.8 Single- Use Bronchoscope System GlideScope® BladderScan® Prime Plus Console, BladderScan® i10™ BladderScan® i10™System, US Probe, BladderScan® i10™ BladderScan® BVI 6400 BladderScan® BVI 6000 Series BladderScan® BVI 6100 GlideScope® BFlex™ 5.8 Single-Use Bronchoscope System GlideScope® BFlex™ Single-Use Bronchoscope System GlideRite® Rigid Stylet FloPoint® Elite

Establishment Types

Manufacture Medical Device Repack or Relabel Medical Device