Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3041915827

FEI Number

3041915827

Entity Name

NOVATECH SCIENTIFIC LLC

City/State/Country

Boca Raton, FL, US

Establishment Address

399 Nw 2nd Ave Ste 216, Boca Raton, FL 33432, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

NovaTech Scientific (Owner Number: 10094103)

Owner / Operator Contact Address

399 NW 2nd Ave, Ste 216, Boca Raton, FL 33432, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NovaTech Percutaneous Discectomy Kit BiDisk Percutaneous Discectomy Kit BIDISK KIT 17G

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HRX	Arthroscope	Orthopedic	Class 2	888.1100	2025-11-14

Official Correspondent

Gabriel Campos

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NovaTech Scientific

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

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 3041915827. Last updated year: 2026. Please use registration number 3041915827 when referencing this establishment in official correspondence.