Contract manufacturerGREGORY MFG., INC. (Holyoke, MA)MassachusettsCardiovascularGeneral hospitalPhysical medicineClass IIClass I
GREGORY MFG., INC.
Contract manufacturer ยท Holyoke, MA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1222630 (openFDA record; or search FDA's registration database)
- FEI number
- 1000120897
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- GREGORY MFG., INC. (FDA owner/operator no. 9002054)
- Registered address
- 102 Cabot St, Holyoke, MA 01040
- Contract listings
- 6 device listings, 6 product codes, first listed Apr 30, 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 |
|---|---|---|---|---|---|
| DXQ | Blood Pressure Cuff | Class II | Cardiovascular | Contract manufacturing | May 18, 2017 |
| FMP | Protector, Skin Pressure | Class I | General hospital | Contract manufacturing | Nov 3, 2015 |
| IME | Pack, Hot Or Cold, Reusable | Class I | Physical medicine | Contract manufacturing | Jun 18, 2014 |
| IRP | Massager, Powered Inflatable Tube | Class II | Physical medicine | Contract manufacturing | Jun 18, 2014 |
| MWI | Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | Class II | Cardiovascular | Contract manufacturing | Jun 12, 2017 |
| OED | Antimicrobial Blood Pressure Cuff | Class II | Cardiovascular | Contract manufacturing | Apr 30, 2013 |