Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010741366

FEI Number

3010741366

Entity Name

INTERSURGICAL S.P.A.

City/State/Country

Mirandola (MO) Italy Modena, IT

Establishment Address

Via Tonino Morandi, 12, Mirandola (MO) Italy Modena 41037, IT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Intersurgical S.p.A. (Owner Number: 10077794)

Owner / Operator Contact Address

Via Tonino Morandi, 12, Mirandola (MO) Italy, IT-MO 41037, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CP903 CAP, STR/019

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ECB	Unit, Syringe, Air And/Or Water	Dental	Class 1	872.4565	2020-09-23
BZA	Connector, Airway (Extension)	Anesthesiology	Class 1	868.5810	2020-09-23

Official Correspondent

Ivan Seniut

US Agent Details

Kerrie Campbell Business: Intersurgical Inc Email: kcampbell@intersurgicalinc.com Phone: (315) 4512900

Related Public Records

Same Entity

Intersurgical S.p.A.

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 3010741366. Last updated year: 2026. Please use registration number 3010741366 when referencing this establishment in official correspondence.