Contract manufacturerMedicraft Inc (Elmwood Park, NJ)New JerseyGeneral and plastic surgeryGeneral hospitalOrthopedicClass IClass II
Medicraft Inc
Contract manufacturer ยท Elmwood Park, NJ
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3009538923 (openFDA record; or search FDA's registration database)
- FEI number
- 3009538923
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Medicraft Inc/Creighton (FDA owner/operator no. 10042540)
- Registered address
- 50 Bushes Ln, Elmwood Park, NJ 07407
- Contract listings
- 5 device listings, 5 product codes, first listed Dec 6, 2012
- 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 | Apr 8, 2020 |
| KCT | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories | Class II | General hospital | Contract manufacturing | Nov 18, 2022 |
| LRP | Tray, Surgical | Class I | General and plastic surgery | Contract manufacturing | Dec 6, 2012 |
| MDM | Instrument, Manual, Surgical, General Use | Class I | General and plastic surgery | Contract manufacturing | Feb 1, 2023 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | Class II | Orthopedic | Contract manufacturing | Jun 20, 2023 |