Contract manufacturerM4D LLC (Lake Forest, CA)CaliforniaCardiovascularGeneral and plastic surgeryNeurologyClass IIHDE
M4D LLC
Contract manufacturer · Lake Forest, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3013858269 (openFDA record; or search FDA's registration database)
- FEI number
- 3013858269
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- M4D LLC (FDA owner/operator no. 10056346)
- Registered address
- 105 North Pointe Drive, Lake Forest, CA 92630
- Contract listings
- 5 device listings, 5 product codes, first listed Dec 12, 2022
- 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 |
|---|---|---|---|---|---|
| DQY | Catheter, Percutaneous | Class II | Cardiovascular | Contract manufacturing | May 20, 2026 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | Class II | General and plastic surgery | Contract manufacturing | May 16, 2024 |
| KRA | Catheter, Continuous Flush | Class II | Cardiovascular | Contract manufacturing | Dec 12, 2022 |
| QJP | Catheter, Percutaneous, Neurovasculature | Class II | Cardiovascular | Contract manufacturing | Sep 23, 2025 |
| QTK | Temporary Percutaneous Transluminal Cerebral Artery Dilatation Device | HDE | Neurology | Contract manufacturing | Jun 22, 2023 |