Kerrie Jiang

FDA Filings

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

FDA Registration(s)

• Registration Number: 3013221323
• FEI Number: 3013221323
• Name: Kerrie Jiang
• Owner & Operator: ZELTIQ Aesthetics, Inc.
• Contact Address: 4410 Rosewood Drive ; Pleasanton CA 94588 US
• Official Correspondent:
  • Kerrie JIANG
  • x-650-7663968-x
• US Agent:
  • Kerrie Jiang
  • Zeltiq Aesthetics, Inc.
  • 925 6212462
  • kerrie.jiang@allergan.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 4410 Rosewood Drive ; Pleasanton, CA 94588 US
• Establishment Type:
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
PMN K120902 | MUU Kerrie Jiang [ZELTIQ Aesthetics, Inc.]	REVOLVE	2019-03-01
PMN K181740 | OOK Kerrie Jiang [ZELTIQ Aesthetics, Inc.]	CoolSculpting System	2018-09-21
PMN K181740 | OOK Kerrie Jiang [ZELTIQ Aesthetics, Inc.]	Accessories: applicator, card, gelpad, gel, gel trap, foam border, liner, strap, skin wipe, gasket, contour	2018-09-21
PMN K171069 | OOK Kerrie Jiang [ZELTIQ Aesthetics, Inc.]	CoolSculpting System	2018-02-05

Similar & Related FDA Registered Companies

• Zeltiq Aesthetics, Inc.