Design Catapult Manufacturing

FDA Filings

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

FDA Registration(s)
Registration Number3015414274
FEI Number3015414274
NameDESIGN CATAPULT MANUFACTURING
Owner & OperatorDesign Catapult Manufacturing
Contact Address3609 W MACARTHUR BLVD STE 805
Santa Ana CA 92704 US
Official Correspondent
  • William Wooten
  • 1-949-5226789-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3609 W MACARTHUR BLVD STE 805
Santa Ana, CA 92704 US
Establishment Type
  • Complaint File Establishment per 21 CFR 820.198
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
DESIGN CATAPULT MANUFACTURING
NXPRO Neuromuscular Electrical Stimulation Device2019-10-15
DESIGN CATAPULT MANUFACTURING
Sensus IORT System2019-04-01
DESIGN CATAPULT MANUFACTURING
SRT-100+2019-04-01
DESIGN CATAPULT MANUFACTURING
SRT-100 Vision2019-04-01
DESIGN CATAPULT MANUFACTURING
SRT-1002019-04-01
DESIGN CATAPULT MANUFACTURING
SILKPEEL; SP DERMALINFUSION2019-03-08

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020080440937Yantian,China (Mainland) -> Los Angeles, CaliforniaALUMINUM DIE CASTING PARTS 0100-8949 275PCS 0100-8948 245 PCS 0100-8947 245PCS 0100-8953 148 PCS 54 CTNS=3 PKGS54 CTN
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