REGENMED SYSTEMS INC.

FDA Device Registration & Listing · Half Moon Bay, CA, US · Registration 3011387885

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
3011387885
FEI Number
3011387885
Entity Name
REGENMED SYSTEMS INC.
City/State/Country
Half Moon Bay, CA, US
Establishment Address
633 Silver Avenue, Half Moon Bay, CA 94019, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
RegenMed Systems Inc. (Owner Number: 10048311)
Owner / Operator Contact Address
106 Oceanview avenue, Half Moon Bay, CA 94019, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MarrowMiner

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GDM Needle, Aspiration And Injection, Reusable General, Plastic Surgery Class 1 878.4800 2014-12-29

Official Correspondent

Michael Crocker

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RegenMed Systems Inc.
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 3011387885. Last updated year: 2026. Please use registration number 3011387885 when referencing this establishment in official correspondence.
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