Contract manufacturerLifeNet Health (Plainfield, IN)IndianaGeneral and plastic surgeryOrthopedicClass IIClass I
LifeNet Health
Contract manufacturer ยท Plainfield, IN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3015724777 (openFDA record; or search FDA's registration database)
- FEI number
- 3015724777
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer for export only; Manufacturer; Contract manufacturer
- Owner or operator
- LIFENET HEALTH (FDA owner/operator no. 9079121)
- Registered address
- 845 Airtech Parkway, Suite 198, Plainfield, IN 46168
- Contract listings
- 4 device listings, 6 product codes, first listed Aug 27, 2007
- 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 |
|---|---|---|---|---|---|
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene | Class II | General and plastic surgery | Contract manufacturing | Aug 27, 2007 |
| GEY | Motor, Surgical Instrument, Ac-Powered | Class I | General and plastic surgery | Contract manufacturing | Jan 30, 2013 |
| HWC | Screw, Fixation, Bone | Class II | Orthopedic | Contract manufacturing | Sep 24, 2024 |
| MAI | Fastener, Fixation, Biodegradable, Soft Tissue | Class II | Orthopedic | Contract manufacturing | Sep 24, 2024 |
| MBI | Fastener, Fixation, Nondegradable, Soft Tissue | Class II | Orthopedic | Contract manufacturing | Sep 24, 2024 |
| OWY | Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon | Class II | General and plastic surgery | Contract manufacturing | Nov 21, 2025 |