Contract manufacturerARCAMED, LLC (Indianapolis, IN)IndianaGeneral and plastic surgeryOrthopedicClass IClass II
ARCAMED, LLC
Contract manufacturer · Indianapolis, IN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3010622588 (openFDA record; or search FDA's registration database)
- FEI number
- 3010622588
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Arcamed, LLC (FDA owner/operator no. 10045595)
- Registered address
- 5101 Decatur Blvd, Suite A, Indianapolis, IN 46241
- Contract listings
- 7 device listings, 6 product codes, first listed Dec 5, 2013
- 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 |
|---|---|---|---|---|---|
| FSM | Tray, Surgical, Instrument | Class I | General and plastic surgery | Contract manufacturing | Dec 5, 2013 |
| HTN | Washer, Bolt Nut | Class II | Orthopedic | Contract manufacturing | May 19, 2026 |
| HWC | Screw, Fixation, Bone | Class II | Orthopedic | Contract manufacturing | May 19, 2026 |
| JDR | Staple, Fixation, Bone | Class II | Orthopedic | Contract manufacturing | May 19, 2026 |
| LRP | Tray, Surgical | Class I | General and plastic surgery | Contract manufacturing | Dec 22, 2015 |
| LXH | Orthopedic Manual Surgical Instrument | Class I | Orthopedic | Contract manufacturing | Mar 4, 2026 |