Compression Solutions, LLC

FDA Device Registration & Listing · Charlotte, NC, US · Registration 3008902816

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
3008902816
FEI Number
3008902816
Entity Name
Compression Solutions, LLC
City/State/Country
Charlotte, NC, US
Establishment Address
5825 Carnegie Blvd,, Suite 300, Charlotte, NC 28209, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Compression Solutions, LLC (Owner Number: 10035499)
Owner / Operator Contact Address
5825 Carnegie Blvd, STE 300, Charlotte, NC 28209, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Triple Play Pro Facility Compression Pump - TPVT-01P Triple Play Pro Facility Compression Pump - TPVT-01PVQ Triple Play EZ-FIT VT Leg Sleeve Extension Panels - TP-3636-EXTVQ Tprile Play EZ-FIT VT Calf Wrap Extension Panels - TP-3333-EXT Triple Play EZ-Fit VT Compression Leg Sleeve - TP-3636s Triple Play EZ-Fit VT Compression Foot Sleeve - TP-3434VQ Triple Play EZ-Fit VT Compression Leg Sleeve - TP-3636sVQ Triple Play EZ-FIT VT Calf Wrap Extension Panels - TP-3333-EXTVQ Triple Play EZ-Fit VT Compression Foot Sleeve - TP-3434 Triple Play EZ-FIT VT Leg Sleeve Extension Panels - TP-3636-EXT Triple Play VT - TP-6480 - Universal Lumbar Orthosis Triple Play VT - TP-6500 - Universal Lumbar Orthosis Triple Play VT - TP-8686 - Boot Walker and Universal Ankle Orthosis Triple Play VT - TP-4453 - Long ROM Knee Orthosis Triple Play VT - TP-4451 - Universal Short ROM Brace Triple Play VT - TP-7777 - Universal Hip Orthosis Triple Play VT - TP-2222 - Universal Elbow Orthosis Triple Play VT - TP-6420 - Universal Lumbar Orthosis Triple Play VT - TP-8888 - Universal Ankle Orthosis Triple Play VT - TP-7751 - Universal Hip Abduction ROM Brace Triple Play VT - TP-4444 - Universal Knee Orthosis Triple Play VT - TP-5555 - Universal Shoulder Orthosis PowerPlay - Cold Compression ROM Knee Brace with One Gel Pack PowerPlay - PPFL-27 Full Leg Cold and Compression Wrap PowerPlay - PPWR-68U Universal Wrist Orthosis PowerPlay - PPKN-360 Circumferential Knee Orthosis PowerPlay - PPHP-65 Universal Hip Orthosis PowerPlay - PPSH-59 Universal Shoulder Orthosis PowerPlay - PPBB-SBP Cold and Compression Back Wrap with One Gel Pack PowerPlay - PPBB-SP Cold and Compression Back Wrap with One Gel Pack PowerPlay - PPKN-58 Cold and Compression Knee Wrap PowerPlay - PPEL-22 Universal Elbow Orthosis PowerPlay - PPAN-66 Universal Ankle Orthosis PowerPlay - PPBB-LBP Cold and Compression Back Wrap with One Gel Pack

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOW Sleeve, Limb, Compressible Cardiovascular Class 2 870.5800 2014-12-15
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2012-01-20

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Compression Solutions, LLC
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

Similar Registrations

Registration Number Establishment Name Location
3033981998 KOYA MEDICAL, INC. Dallas, TX, US
3020703724 Therma Bright Inc. Toronto Ontario, CA
3014491159 AIROS MEDICAL INC Audubon, PA, US
3014834638 ZENITH TECHNICAL INNOVATIONS, LLC Gurnee, IL, US
3009155917 GRANDWAY TECHNOLOGY (SHENZHEN) LIMITED Shenzhen Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008902816. Last updated year: 2026. Please use registration number 3008902816 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.