Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014200871

FEI Number

3014200871

Entity Name

ADRIA SRL.

City/State/Country

San Giovanni in Persiceto Bologna, IT

Establishment Address

Via Modena n. 46, San Giovanni in Persiceto Bologna 40017, IT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Adria Srl. (Owner Number: 10062522)

Owner / Operator Contact Address

Via Modena n. 46, San Giovanni in Persiceto (BO), IT-NOTA 40017, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Herniatome 5091715, 5091749, 5091745 Cement Injection Cannula - 495041420 Kit of 2 Cement delivery instruments - 495041123 Vertebroplasty Injector Kit - 49000001 Hollow Drill - 495930810 Litebag 500/0600 Vertebroplasty Needle Kit - 49225 Vertebroplasty Needle - 496xx, 498xx, 491xx, 490xx, 492xx, T0604xx Vertebroplasty Canulated Needle - 493xx, T0604xx

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HRX	Arthroscope	Orthopedic	Class 2	888.1100	2020-02-06
OAR	Injector, Vertebroplasty (Does Not Contain Cement)	Orthopedic	Class 1	888.4200	2025-01-21
HTW	Bit, Drill	Orthopedic	Class 1	888.4540	2025-01-21
KNX	Collector, Urine, (And Accessories) For Indwelling Catheter	Gastroenterology, Urology	Class 2	876.5250	2022-12-01
OCJ	Spinal Channeling Instrument, Vertebroplasty	Orthopedic	Class 1	888.4540	2025-01-21

Official Correspondent

No official correspondent registered.

US Agent Details

Duc Duong Business: Dumotech, LLC. Email: dduong@dumotech.com Phone: (800) 9196101

Related Public Records

Same Entity

Adria Srl.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K081051	Spine View, Inc.	SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS), SPINEVU MINISCOPE	2008-08-07
K820777	The Anspach Effort, Inc.	MINI-MICRO ARTHROSCOPIC SCAPEL	1982-05-12
K791969	Medline Industries, Inc.	DYNACOR STERILE CLOSED SYS. DRAINAGE BAG	1979-11-05

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0041-05	Linvatec Corp.	2	Ultra Power Burs, Sterile, Single-Use.

Similar Registrations

Registration Number	Establishment Name	Location
3044858680	JIENO YOUCHENG MEDICAL TECHNOLOGY (SHANGHAI) CO., LTD.	Shanghai, CN
1650907	Isomedix Operations Inc.	GRAND PRAIRIE, TX, US
3014615697	AMNOTEC INTERNATIONAL MEDICAL GMBH	Neuhausen ob Eck Baden-Wurttemberg, DE
3043226252	ZAPALIGN LLC	Fort Lauderdale, FL, US
3020978007	DONGGUAN BAO KANG DIAN ZI KE JI LIMITED	Dongguan City Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014200871. Last updated year: 2026. Please use registration number 3014200871 when referencing this establishment in official correspondence.