GYNESONICS, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30058756753005875675GYNESONICS, INC.1N2026-01-01200 Cardinal Way #250 REDWOOD CITY CA US 94063
30058756753005875675GYNESONICS, INC.1N2020-04-25600 Chesapeake Drive REDWOOD CITY CA US 94063

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
10817929020241Sonata® Intrauterine Ultrasound Probe - Ultrasound-guided intrauterine electrosurgical diathermy system intrauterine ultrasound transducer, Sterile650-216-3860customersupport@gynesonics.com
10817929020357Sonata® System Software - Ultrasound-guided radio-frequency ablation system software650-216-3860customersupport@gynesonics.com
10817929020364Sonata® Dispersive Electrode - Electrosurgical return electrode, single-use650-216-3860UScustomerservice@gynesonics.com
10817929020371Sonata® Radiofrequency Ablation Handpiece - Ultrasound-guided intrauterine electrosurgical handpiece/ electrode1-650-216-3860UScustomerservice@gynesonics.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3420451961946932K250705Sonata Transcervical Fibroid Ablation System 2.2KNF2025-04-02
3420451318492505K240503Sonata Transcervical Fibroid Ablation System 2.2KNF2024-07-17
3420451061407327K222304Sonata Transcervical Fibroid Ablation System 2.2KNF2022-11-08
3420451181664826K211535Sonata Transcervical Fibroid Ablation System 2.2KNF2021-06-17
666552044431334K173703Sonata Sonography-Guided Transcervical Fibroid Ablation SystemKNF2018-08-15

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KNF52025-04-02

PMN#

GUDID#