Richard Hurst

FDA Filings

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

FDA Registration(s)
Registration Number3008034554
FEI Number3008034554
NameRichard Hurst
Owner & OperatorXL Precision Technologies Ltd
Contact Address79 Sadler Forster Way
Stockton on Tees GB-STT Stockton-on-Tees TS17 9JY GB
Official Correspondent
  • Alan T Graham
  • 44-1642-766960-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address19 Hagerty Boulevard Suite C
West Chester, PA 19382 US
Establishment TypeExport Device to the United States But Perform No Other Operation on Device



FDA Filings

Device
Company
DeviceDate
Richard Hurst [XL Precision Technologies Ltd]
ToggleLoc 2.9 and JuggerLoc Soft Tissue System2020-01-15
Richard Hurst [XL Precision Technologies Ltd]
ToggleLoc 2.9 and JuggerLoc Soft Tissue System2020-01-15
Richard Hurst [XL Precision Technologies Ltd]
Hydrodam Re-usable Obturator Shaft 8.5mm2019-07-03
Richard Hurst [XL Precision Technologies Ltd]
Hydrodam Re-usable Obturator Shaft 7.0mm2019-07-03
Richard Hurst [XL Precision Technologies Ltd]
Hydrodam Re-usable Obturator Shaft 5mm2019-07-03
Richard Hurst [XL Precision Technologies Ltd]
Hydrodam Re-usable Obturator Handle2019-07-03

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