Contract manufacturerLIFECYCLE BIOTECHNOLOGIES, LLC (Cleburne, TX)TexasGastroenterology and urologyClass II
LIFECYCLE BIOTECHNOLOGIES, LLC
Contract manufacturer ยท Cleburne, TX
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3020224798 (openFDA record; or search FDA's registration database)
- FEI number
- 3010877980
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- Lifecycle Biotechnologies, LP (FDA owner/operator no. 10049711)
- Registered address
- 421 Marti Drive, Cleburne, TX 76033
- Contract listings
- 3 device listings, 2 product codes, first listed Aug 18, 2025
- 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 |
|---|---|---|---|---|---|
| KDL | Set, Perfusion, Kidney, Disposable | Class II | Gastroenterology and urology | Contract manufacturing | Nov 21, 2025 |
| KDN | System, Perfusion, Kidney | Class II | Gastroenterology and urology | Contract manufacturing | Aug 18, 2025 |