Contract manufacturerDESIGN CATAPULT MANUFACTURING (Fountain Valley, CA)CaliforniaObstetrics and gynecologyPhysical medicineClass IClass II
DESIGN CATAPULT MANUFACTURING
Contract manufacturer ยท Fountain Valley, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3015414274 (openFDA record; or search FDA's registration database)
- FEI number
- 3015414274
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Design Catapult Manufacturing (FDA owner/operator no. 10059922)
- Registered address
- 17331 Newhope Street, Fountain Valley, CA 92708
- Contract listings
- 2 device listings, 2 product codes, first listed Oct 15, 2019
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| LHQ | System, Telethermographic (Adjunctive Use) | Class I | Obstetrics and gynecology | Contract manufacturing | Dec 10, 2024 |
| NGX | Stimulator, Muscle, Powered, For Muscle Conditioning | Class II | Physical medicine | Contract manufacturing | Oct 15, 2019 |