SYNTHON HISPANIA S.L.

FDA Device Registration & Listing · Sant Boi de Llobregat Barcelona, ES · Registration 3004837462

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
3004837462
FEI Number
3004837462
Entity Name
SYNTHON HISPANIA S.L.
City/State/Country
Sant Boi de Llobregat Barcelona, ES
Establishment Address
CALLE Castello, 1 - PG SALINAS, Sant Boi de Llobregat Barcelona 08830, ES
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Synthon Hispania S.L. (Owner Number: 10092498)
Owner / Operator Contact Address
Castello 1, Sant Boi de Llobregat, ES-B 08830, ES
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K243232
PMA Number
N/A

All Registered Proprietary Names

GripMate

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KZH Introducer, Syringe Needle General Hospital Class 2 880.6920 2025-01-15

Official Correspondent

Ana Miralles

US Agent Details

Rebecca (Becky) Welton Business: Lachman Consultant Services, Inc. Email: lcsreg@lachmanconsultants.com Phone: (516) 2226222

Related Public Records

Same Entity

Synthon Hispania S.L.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004837462. Last updated year: 2026. Please use registration number 3004837462 when referencing this establishment in official correspondence.
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