Kehr Surgical Allied Products

FDA Filings

This page includes the latest FDA filings for Kehr Surgical Allied Products. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3004971305
• FEI Number: 3004971305
• Name: Megan Slocum
• Owner & Operator: KEHR SURGICAL & ALLIED PRODUCTS
• Contact Address: C 34 PANKI INDUSTRIAL ESTATE --; KANPUR, UP IN-NOTA 208022 IN
• US Agent:
  • Megan Slocum
  • Emergo by UL
  • 512 3279997
  • 512 3279998
  • usagent@ul.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 2500 Bee Cave Road Bldg 1, Suite 300; Austin, TX 78746 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GES Megan Slocum [KEHR SURGICAL & ALLIED PRODUCTS]	Surgeon	2005-01-18
GES Megan Slocum [KEHR SURGICAL & ALLIED PRODUCTS]	KIATO	2005-01-18
GES Megan Slocum [KEHR SURGICAL & ALLIED PRODUCTS]	KIATO Plus	2005-01-18
GDZ Megan Slocum [KEHR SURGICAL & ALLIED PRODUCTS]	KIATO	2005-01-18
GDX Megan Slocum [KEHR SURGICAL & ALLIED PRODUCTS]	KIATO	2005-01-18
GDX Megan Slocum [KEHR SURGICAL & ALLIED PRODUCTS]	KIATO Plus	2005-01-18
GDH Megan Slocum [KEHR SURGICAL & ALLIED PRODUCTS]	KIATO GOUGE BLADE	2005-01-18