HATCH PRODUCT DEVELOPMENT LLC

FDA Device Registration & Listing · Waukegan, IL, US · Registration 3030438338

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3030438338
FEI Number
3030438338
Entity Name
HATCH PRODUCT DEVELOPMENT LLC
City/State/Country
Waukegan, IL, US
Establishment Address
2330 ERNIE KRUEGER CIRCLE, Waukegan, IL 60087, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Hatch Product Development LLC (Owner Number: 10090588)
Owner / Operator Contact Address
2330 ERNIE KRUEGER CIRCLE, Waukegan, IL 60087, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

XSONX WHS XSONX Wound Hygiene System SIMPULL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2025-12-17
FRZ Device, Patient Transfer, Powered General Hospital Class 2 880.6775 2024-04-16

Official Correspondent

Brad Teck

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hatch Product Development LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030438338. Last updated year: 2026. Please use registration number 3030438338 when referencing this establishment in official correspondence.
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