Apmtd Inc

FDA Filings

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

FDA Registration(s)

• Registration Number: 3015431638
• FEI Number: 3015431638
• Name: APMTD, INC.
• Owner & Operator: APMTD, Inc.
• Contact Address: One Broadway, 14th Floor ; Cambridge MA 02142 US
• Official Correspondent:
  • John Sasso
  • 1-781-9626274-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: One Broadway, 14th Floor ; Cambridge, MA 02142 US
• Establishment Type: Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device Company	Device	Date
GUDID 00850000067134 APMTD, Inc.	Anivia SG1000 Pump Console SG1000-LSM-001	2024-09-19
GUDID 00850000067127 APMTD, Inc.	Anivia SG1000 Pump Console SG1000-CRT-001	2024-09-19
GUDID 00850000067110 APMTD, Inc.	Anivia SG1000 Pump Console SG1000-FBS-002	2024-09-19
GUDID 00850000067103 APMTD, Inc.	Anivia SG1000 Pump Console SG1000-FBS-001	2024-09-19
GUDID 00850000067097 APMTD, Inc.	Anivia SG1000 Pump Console SG1000-PDM-004	2024-09-19
GUDID 00850000067080 APMTD, Inc.	Anivia SG1000 Pump Console SG1000-PDM-003	2024-09-19
GUDID 00850000067073 APMTD, Inc.	Anivia SG1000 Pump Console SG1000-PDM-002	2024-09-19
GUDID 00850000067066 APMTD, Inc.	Anivia SG1000 Pump Console SG1000-PDM-001	2024-09-19
GUDID 00850000067059 APMTD, Inc.	Anivia SG1000 Pump Console SG1000-DCM-001	2024-09-19
KMK APMTD, INC.	wClamp	2019-03-25
KGX APMTD, INC.	Skin Tab	2019-03-25