Contract manufacturerBLUR PRODUCT DEVELOPMENT (Cary, NC)North CarolinaGastroenterology and urologyGeneral and plastic surgeryRadiologyClass IIClass INot classified
BLUR PRODUCT DEVELOPMENT
Contract manufacturer ยท Cary, NC
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3014644251 (openFDA record; or search FDA's registration database)
- FEI number
- 3014644251
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Blur Development Group (FDA owner/operator no. 10087809)
- Registered address
- 260 James Jackson Ave., Cary, NC 27513
- Contract listings
- 3 device listings, 3 product codes, first listed Apr 12, 2023
- 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 |
|---|---|---|---|---|---|
| EXY | Uroflowmeter | Class II | Gastroenterology and urology | Contract manufacturing | Jun 25, 2025 |
| FSO | Microscope, Surgical, General & Plastic Surgery | Class I | General and plastic surgery | Contract manufacturing | Oct 30, 2023 |
| QVW | Generator, Measurement, And/Or Delivery System For Hyperpolarized Mr Imaging Agents And Accessories, Cder Or Cber-Led | Not classified | Radiology | Contract manufacturing | Apr 12, 2023 |