YOURBIO HEALTH

FDA Device Registration & Listing · Minnetonka, MN, US · Registration 3039524238

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
3039524238
FEI Number
3039524238
Entity Name
YOURBIO HEALTH
City/State/Country
Minnetonka, MN, US
Establishment Address
5421 Feltl Rd Ste 190, Minnetonka, MN 55343, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device
Owner / Operator
YourBio Health, Inc (Owner Number: 10055725)
Owner / Operator Contact Address
5421 Feltl Road, Suite 190, Minnetonka, MN 55343, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

TAP Micro Select

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature General, Plastic Surgery Class 2 878.4850 2023-05-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K130132 Medipurpose Pte. , Ltd. BABYLANCE HEEL INCISION DEVICE 2013-02-11

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0044-2008 Becton Dickinson & Company 2
Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039524238. Last updated year: 2026. Please use registration number 3039524238 when referencing this establishment in official correspondence.
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