Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011541120

FEI Number

3011541120

Entity Name

AGUPUNT S.L.

City/State/Country

Barcelona, ES

Establishment Address

C/ Caspe 158, Barcelona E-08013, ES

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

AGUPUNT S.L. (Owner Number: 10048785)

Owner / Operator Contact Address

C/ Caspe 158, Barcelona, ES-B E-08013, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Physiotherapy Needles Agu-Punt SL Agupunt USA Corp Agupunt Agupunt USA Corp

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQX	Needle, Acupuncture, Single Use	General Hospital	Class 2	880.5580	2015-02-27
GDF	Guide, Needle, Surgical	General, Plastic Surgery	Class 1	878.4800	2023-10-26

Official Correspondent

Oriol Cuch

US Agent Details

Oriol Cuch Business: Agupunt USA Corp Email: oriol@agugroup.com Phone: (305) 4609078

Related Public Records

Same Entity

AGUPUNT 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 3011541120. Last updated year: 2026. Please use registration number 3011541120 when referencing this establishment in official correspondence.