MOBIUS BIONICS LLC

FDA Device Registration & Listing · Manchester, NH, US · Registration 3012481940

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
3012481940
FEI Number
3012481940
Entity Name
MOBIUS BIONICS LLC
City/State/Country
Manchester, NH, US
Establishment Address
286 COMMERCIAL ST, Manchester, NH 03101, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Mobius Bionics LLC (Owner Number: 10051633)
Owner / Operator Contact Address
286 Commercial St., Manchester, NH 03101, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
DEN120016
PMA Number
N/A

All Registered Proprietary Names

DEKA Arm System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PAE Upper Extremity Prosthesis With Multiple Simultaneous Degrees Of Freedom And Controlled Via Cutaneous Electromyography Physical Medicine Class 2 890.3450 2016-04-14

Official Correspondent

Joseph Sullivan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mobius Bionics LLC
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 3012481940. Last updated year: 2026. Please use registration number 3012481940 when referencing this establishment in official correspondence.
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