SWAN MEDICAL SL

FDA Device Registration & Listing · Barcelona, ES · Registration 3016851779

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
3016851779
FEI Number
3016851779
Entity Name
SWAN MEDICAL SL
City/State/Country
Barcelona, ES
Establishment Address
C/ Corcega 270 3o2a, Port Ginesta Local 814, Modulo B, Barcelona 08008, ES
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SWAN MEDICAL SL (Owner Number: 10092571)
Owner / Operator Contact Address
C/ Corcega 270 3o2a, Port Ginesta Local 814, Modulo B, Barcelona, ES-B 08008, ES
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Rutilight Rutilight power supply Rutiside

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FSQ Light, Surgical, Instrument General, Plastic Surgery Class 2 878.4580 2025-01-22

Official Correspondent

Jose Antonio Navas

US Agent Details

Rodrigo Abreu Business: United Regulatory & Logistics LLC Email: rabreu@unitedregulatory.com Phone: (786) 2667900

Related Public Records

Same Entity

SWAN MEDICAL SL
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 3016851779. Last updated year: 2026. Please use registration number 3016851779 when referencing this establishment in official correspondence.
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