Contract manufacturerWASATCH PRODUCT DEVELOPMENT, LLC (Draper, UT)UtahNeurologyGeneral and plastic surgeryObstetrics and gynecologyClass IIClass I
WASATCH PRODUCT DEVELOPMENT, LLC
Contract manufacturer · Draper, UT
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3003676119 (openFDA record; or search FDA's registration database)
- FEI number
- 3003676119
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- Wasatch Product Development LLC (FDA owner/operator no. 10055790)
- Registered address
- 427 W 11950 S, Draper, UT 84020
- Contract listings
- 3 device listings, 3 product codes, first listed Oct 6, 2017
- 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 |
|---|---|---|---|---|---|
| GYB | Media, Electroconductive | Class II | Neurology | Contract manufacturing | Dec 10, 2021 |
| NAE | Dressing, Wound, Hydrogel Without Drug And/Or Biologic | Class I | General and plastic surgery | Contract manufacturing | Oct 6, 2017 |
| NUC | Lubricant, Personal | Class II | Obstetrics and gynecology | Contract manufacturing | Feb 27, 2020 |