EHMET HEALTH

FDA Device Registration & Listing · Plymouth, MI, US · Registration 3016872563

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
3016872563
FEI Number
3016872563
Entity Name
EHMET HEALTH
City/State/Country
Plymouth, MI, US
Establishment Address
47801 W Anchor Ct, Plymouth, MI 48170, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Ehmet Health (Owner Number: 10073828)
Owner / Operator Contact Address
47801 W Anchor Ct, Plymouth, MI 48170, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K181498
PMA Number
N/A

All Registered Proprietary Names

X-ray Imaging System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LHN System, Radiation Therapy, Charged-Particle, Medical Radiology Class 2 892.5050 2020-05-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ehmet Health
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0014-2009 Intraop Medical Corporation 2
Mobetron Model 1000, mobile electron linear accelerator, a device system which delivers radiation to an intraoperative site.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016872563. Last updated year: 2026. Please use registration number 3016872563 when referencing this establishment in official correspondence.
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