Contract manufacturerHATCH PRODUCT DEVELOPMENT LLC (Wauconda, IL)IllinoisGeneral hospitalGeneral and plastic surgeryClass IIClass I
HATCH PRODUCT DEVELOPMENT LLC
Contract manufacturer ยท Wauconda, IL
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3030438338 (openFDA record; or search FDA's registration database)
- FEI number
- 3030438338
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Hatch Product Development LLC (FDA owner/operator no. 10090588)
- Registered address
- 1200 Karl Ct, Wauconda, IL 60084
- Contract listings
- 2 device listings, 2 product codes, first listed Apr 16, 2024
- 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 |
|---|---|---|---|---|---|
| FRZ | Device, Patient Transfer, Powered | Class II | General hospital | Contract manufacturing | Apr 16, 2024 |
| GFE | Brush, Dermabrasion, Powered | Class I | General and plastic surgery | Contract manufacturing | Dec 17, 2025 |