Contract manufacturerHubot, Inc. (South Bend, IN)IndianaGeneral and plastic surgeryPhysical medicineClass IIUnclassified
Hubot, Inc.
Contract manufacturer ยท South Bend, IN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3015177815 (openFDA record; or search FDA's registration database)
- FEI number
- 3015177815
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Hubot, Inc. (FDA owner/operator no. 10058602)
- Registered address
- 3333 N. Kenmore St, South Bend, IN 46628
- Contract listings
- 4 device listings, 2 product codes, first listed Oct 12, 2021
- 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 |
|---|---|---|---|---|---|
| GEH | Unit, Cryosurgical, Accessories | Class II | General and plastic surgery | Contract manufacturing | Oct 12, 2021 |
| MLY | Vapocoolant Device | Unclassified | Physical medicine | Contract manufacturing | Oct 12, 2021 |