Marox Corp

FDA Filings

This page includes the latest FDA filings for Marox Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 1219213
• FEI Number: 1219213
• Name: MAROX CORP.
• Owner & Operator: MAROX CORP.
• Contact Address: 373 WHITNEY AVENUE --; Holyoke MA 01040 US
• Official Correspondent:
  • MICHAEL - CORATTI
  • x-413-5361300-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 373 WHITNEY AVE. ; HOLYOKE, MA 01040 US
• Establishment Type:
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Manufacture Device in the United States for Export Only

FDA Filings

Device Company	Device	Date
PMN K050369 | NAY MAROX CORP.	da Vinci Xi, Cannula, Reusable	2018-11-30
PMN K121060 | KWQ MAROX CORP.	Indus ACP System	2013-11-15
PMN K093776 | KWQ MAROX CORP.	Indus ACP System	2013-11-15
PMN K130306 | OVE MAROX CORP.	Incite Anchored Cervical Interbody Device	2013-09-18
PMN K122008 | OVE MAROX CORP.	Incite Anchored Cervical Interbody Device	2013-09-18
HRS MAROX CORP.	Trauma	2013-01-22
PMN K050774 | KWQ MAROX CORP.	Snowcap	2012-12-03
PMN K042508 | MNI MAROX CORP.	Mountaineer OCT Spinal System	2012-12-03
PMN K042508 | KWP MAROX CORP.	Mountaineer OCT Spinal System	2012-12-03