Resoundant Inc

FDA Filings

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

FDA Registration(s)

• Registration Number: 3013695852
• FEI Number: 3013695852
• Name: RESOUNDANT, INC.
• Owner & Operator: Resoundant, Inc.
• Contact Address: 421 1st Ave SW STE 204W ; Rochester MN 55902 US
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 421 1st Ave SW STE 204W ; Rochester, MN 55902 US
• Establishment Type:
  • Develop Specifications But Do Not Manufacture At This Facility
  • Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 00850011790267 RESOUNDANT, INC.	Active Driver v2	2025-09-11
GUDID 00850011790229 RESOUNDANT, INC.	Pillow Passive Driver Kit	2024-10-11
GUDID 00850011790052 RESOUNDANT, INC.	Flex Passive Driver Kit- Small	2023-04-10
GUDID 00850011790045 RESOUNDANT, INC.	Flex Passive Driver Kit- Large	2023-04-10
GUDID 00850011790106 RESOUNDANT, INC.	Passive Driver	2023-03-01
GUDID 00850011790199 RESOUNDANT, INC.	Hepatogram Plus MREPLUSV3	2022-04-21
GUDID 00850011790014 RESOUNDANT, INC.	MREplus	2021-04-09
GUDID 00850011790007 RESOUNDANT, INC.	MREplus	2021-04-09
PMN K201389 Resoundant Inc	Resoundant Acoustic Driver System	2020-07-10
PMN K183193 | LLZ RESOUNDANT, INC.	MREplus+	2019-08-21
PMN K183193 Resoundant Inc	MREplus+ Software	2019-08-01
IXF RESOUNDANT, INC.	Resoundant	2017-05-14