HINCKLEY MEDICAL, INC. dba ONEDOSE

FDA Device Registration & Listing · Bloomington, MN, US · Registration 3027485564

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
3027485564
FEI Number
3027485564
Entity Name
HINCKLEY MEDICAL, INC. dba ONEDOSE
City/State/Country
Bloomington, MN, US
Establishment Address
4801 W 81st St Ste 118, Bloomington, MN 55437, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Hinckley Medical, Inc. dba OneDose (Owner Number: 10088266)
Owner / Operator Contact Address
4801 W 81st St, STE 118, Bloomington, MN 55437, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ONEWEIGHT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRW Scale, Patient General Hospital Class 1 880.2720 2023-06-21

Official Correspondent

Michael Elsbernd

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hinckley Medical, Inc. dba OneDose
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 3027485564. Last updated year: 2026. Please use registration number 3027485564 when referencing this establishment in official correspondence.
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