FDA.reportPublic FDA data

REBOUND THERAPEUTICS, CORPORATION

Matched from indexed company URL: REBOUND THERAPEUTICS CORPORATION

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30135056383013505638REBOUND THERAPEUTICS, CORPORATION1N2026-01-0113900 Alton Parkway Suite 120 Irvine CA US 92618

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00850002332049AURORA® Surgiscope® - AURORA® Surgiscope® System Power Cable+1(800)654-2873custsvcnj@integralife.com
00850002332148AURORA® - AURORA® Evacuator Outer Diameter: 10F (3.4mm), Length: 13cm+1(800)654-2873custsvcnj@integralife.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2337231907135968K250752AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80)GWG2025-04-09
2337231476643237K232618Aurora Surgiscope SystemGWG2023-10-27
2337231442462468K203745AURORA Evacuator +CoagGEI2021-12-02
2337231069156317K191861Aurora Surgiscope SystemGWG2019-12-06
2337231733388089K190075Aurora EvacuatorGEI2019-02-12
2337232039690774K182211Aurora Surgiscope SystemGWG2019-01-18
2337231424809252K180372Aurora EvacuatorGEI2018-04-09

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GWG42025-04-09
GEI32021-12-02

PMN#

GUDID#