ENOPREP, Inc

FDA Device Registration & Listing · Big Canoe, GA, US · Registration 3042617566

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
3042617566
FEI Number
3042617566
Entity Name
ENOPREP, Inc
City/State/Country
Big Canoe, GA, US
Establishment Address
655 Turnbury Lane, 12120 Big Canoe, Big Canoe, GA 30143, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
EnOPrep, Inc. (Owner Number: 10094597)
Owner / Operator Contact Address
2135 Westwood Rd, Smyrna, GA 30080, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Enoprep

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OHY Pill Crusher/Cutter General Hospital Class 1 880.6430 2025-12-09

Official Correspondent

Ward Broom

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EnOPrep, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042617566. Last updated year: 2026. Please use registration number 3042617566 when referencing this establishment in official correspondence.
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