Savantini Holdings Limited

FDA Device Registration & Listing · Hull East Riding of Yorkshire, GB · Registration 3006897018

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3006897018
FEI Number
3006897018
Entity Name
Savantini Holdings Limited
City/State/Country
Hull East Riding of Yorkshire, GB
Establishment Address
Savantini House, Foster Street, Hull East Riding of Yorkshire HU8 8BT, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Savantini Holdings Limited (Owner Number: 10024217)
Owner / Operator Contact Address
Savantini House, Foster Street, Kingston Upon Hull, GB-ERY HU8 8BT, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K081480
PMA Number
N/A

All Registered Proprietary Names

Kegel8 Ultra Core

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPI Stimulator, Electrical, Non-Implantable, For Incontinence Gastroenterology, Urology Class 2 876.5320 2009-04-29

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Savantini Holdings Limited
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006897018. Last updated year: 2026. Please use registration number 3006897018 when referencing this establishment in official correspondence.
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