Citra Labs L L C

FDA Filings

This page includes the latest FDA filings for Citra Labs L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 1216032
• FEI Number: 1216032
• Name: Citra Labs LLC
• Owner & Operator: Biomet, Inc.
• Contact Address: 56 East Bell Dr. PO Box 587; Warsaw IN 46582 US
• Official Correspondent:
  • Steven C de Baca
  • 1-574-3773437-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 55 Messina Dr ; Braintree, MA 02184 US
• Establishment Type:
  • Complaint File Establishment per 21 CFR 820.198
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
Rejuvesol Citra Labs LLC, Citra Labs, LLC	Prescription Medication	2023-02-15
triCitrasol Citra Labs LLC, Citra Labs, LLC	Prescription Medication	2023-02-15
triCitrasol Citra Labs LLC, Citra Labs, LLC	Prescription Medication	2019-11-21
GUDID 00887868260285 Citra Labs, LLC	Y-Type Rejuvenation Set PN-7212	2019-04-16
triCitrasol Citra Labs LLC, Citra Labs, LLC	Prescription Medication	2018-03-23
PMN K101557 | MQV Citra Labs LLC [Biomet, Inc.]	GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGEN	2018-03-23
PMN K101557 | MBP Citra Labs LLC [Biomet, Inc.]	GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGEN	2018-03-23
Rejuvesol Citra Labs LLC, Citra Labs, LLC	Prescription Medication	2018-02-23
PMN BK950060 | KSB Citra Labs LLC [Biomet, Inc.]	Rejuvesol	2016-12-09
PMN BK950060 | KSB Citra Labs LLC [Biomet, Inc.]	ACD-A	2016-12-09
NDC 23731-6030 Citra Labs LLC	TriCitrasol	2003-07-10
NDC 23731-7000 Citra Labs LLC	Rejuvesol	1997-02-26