Contract manufacturerAquabiliti (Nashville, TN)TennesseeGeneral hospitalClass II
Aquabiliti
Contract manufacturer · Nashville, TN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1057300 (openFDA record; or search FDA's registration database)
- FEI number
- 1000151124
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Manufacturer; Contract manufacturer
- Owner or operator
- MRP, LLC (FDA owner/operator no. 9076844)
- Registered address
- 5209 Linbar Dr Ste 640, Nashville, TN 37211
- Contract listings
- 1 device listings, 1 product codes, first listed May 22, 2014
- 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 |
|---|---|---|---|---|---|
| NGT | Saline, Vascular Access Flush | Class II | General hospital | Contract manufacturing | May 22, 2014 |