Contract manufacturerHiArc (Merrimack, NH)New HampshireHematologyClass II
HiArc
Contract manufacturer · Merrimack, NH
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1219738 (openFDA record; or search FDA's registration database)
- FEI number
- 1219738
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- KMC Systems (FDA owner/operator no. 9024188)
- Registered address
- 220 DANIEL WEBSTER HWY., Merrimack, NH 03054
- Contract listings
- 1 device listings, 3 product codes, first listed Feb 6, 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 |
|---|---|---|---|---|---|
| DAP | Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control | Class II | Hematology | Contract manufacturing | Feb 6, 2013 |
| GGN | Plasma, Coagulation Control | Class II | Hematology | Contract manufacturing | Feb 6, 2013 |
| JPA | System, Multipurpose For In Vitro Coagulation Studies | Class II | Hematology | Contract manufacturing | Feb 6, 2013 |