Contract manufacturerITECH (San Diego, CA)CaliforniaGeneral and plastic surgeryCardiovascularClass IClass III
ITECH
Contract manufacturer · San Diego, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3002714378 (openFDA record; or search FDA's registration database)
- FEI number
- 3002714378
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- iTECH (FDA owner/operator no. 10076088)
- Registered address
- 9454 Waples St, San Diego, CA 92121
- Contract listings
- 3 device listings, 2 product codes, first listed Jul 7, 2020
- 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 |
|---|---|---|---|---|---|
| LYU | Accessory, Surgical Apparel | Class I | General and plastic surgery | Contract manufacturing | Dec 17, 2024 |
| MKJ | Automated External Defibrillators (Non-Wearable) | Class III | Cardiovascular | Contract manufacturing | Jul 7, 2020 |