MEBSTER Inc.

FDA Device Registration & Listing · Baltimore, MD, US · Registration 3032847809

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
3032847809
FEI Number
3032847809
Entity Name
MEBSTER Inc.
City/State/Country
Baltimore, MD, US
Establishment Address
101 W Dickman St, Baltimore, MD 21230, US
Establishment Type(s)
Remanufacture Medical Device,Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
MEBSTER Inc. (Owner Number: 10091573)
Owner / Operator Contact Address
101 West Dickman Street, Baltimore, MD 21230, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

UNILEXA HOME kit 2.1 UNILEXA PRIME 2.1

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2024-10-16

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MEBSTER 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 3032847809. Last updated year: 2026. Please use registration number 3032847809 when referencing this establishment in official correspondence.
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