INVICTUS GLOBAL LIMITED

FDA Device Registration & Listing · SWADLINCOTE Derbyshire, GB · Registration 3017844600

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
3017844600
FEI Number
3017844600
Entity Name
INVICTUS GLOBAL LIMITED
City/State/Country
SWADLINCOTE Derbyshire, GB
Establishment Address
3 - 4 OAKTREE BUSINESS PARK, SWADLINCOTE Derbyshire DE11 9DJ, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
INVICTUS GLOBAL LIMITED (Owner Number: 10079058)
Owner / Operator Contact Address
3 - 5 OAKTREE BUSIENSS PARK, SWADLINCOTE, GB-DBY DE11 9DJ, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FPO Stretcher, Wheeled General Hospital Class 2 880.6910 2020-11-17
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2020-11-17
FMR Device, Transfer, Patient, Manual General Hospital Class 1 880.6785 2020-11-17
NZD Stretcher, Patient Restraint General Hospital Class 1 880.6900 2020-11-17
FPP Stretcher, Hand-Carried General Hospital Class 1 880.6900 2020-11-17

Official Correspondent

Mark Roberts

US Agent Details

ALLEN PERL Email: ap@pgacpa.com Phone: (914) 5230959

Related Public Records

Same Entity

INVICTUS GLOBAL LIMITED
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0023-05 Stryker Medical 2
Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017844600. Last updated year: 2026. Please use registration number 3017844600 when referencing this establishment in official correspondence.
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