Rose Medical

FDA Device Registration & Listing · Grand Rapids, MI, US · Registration 3012977275

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
3012977275
FEI Number
3012977275
Entity Name
Rose Medical
City/State/Country
Grand Rapids, MI, US
Establishment Address
902 Scribner Ave Nw, Grand Rapids, MI 49504, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Rose Medical (Owner Number: 10042209)
Owner / Operator Contact Address
1440 Front Avenue NW, Grand Rapids, MI 49504, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MANTA Depth Locator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MGB Device, Hemostasis, Vascular Unknown Class 3 N/A 2025-01-03

Official Correspondent

Eric Vroegop

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
1836324 Rose Medical Grand Rapids, MI, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012977275. Last updated year: 2026. Please use registration number 3012977275 when referencing this establishment in official correspondence.
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