Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012174974

FEI Number

3012174974

Entity Name

Compedica Limited

City/State/Country

Wyboston Bedford, GB

Establishment Address

The Knowledge Centre, Wyboston Lakes, Great North Rd, Wyboston Bedford MK44 3BY, GB

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Compedica Holdings Limited (Owner Number: 10051096)

Owner / Operator Contact Address

4th Floor, VIking House, Nelson Street, Douglas, IM-NOTA IM1 2AH, IM

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K150806

PMA Number

N/A

All Registered Proprietary Names

PulseFlow Aresta Protective Insole OptiPulse Active Therapy System PulseFlow DF

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KNP	Orthosis, Corrective Shoe	Physical Medicine	Class 1	890.3475	2017-04-08
JOW	Sleeve, Limb, Compressible	Cardiovascular	Class 2	870.5800	2016-02-03

Official Correspondent

No official correspondent registered.

US Agent Details

Patrice McMorrow Email: patrice.mcmorrow@compedica.com Phone: (814) 2084264

Related Public Records

Same Entity

Compedica Holdings Limited

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
K170216	Tactile Systems Technology, Inc. (Dba Tactile Medical)	Flexitouch System	2017-05-26
K100306	Covidien	KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES	2010-05-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012174974. Last updated year: 2026. Please use registration number 3012174974 when referencing this establishment in official correspondence.