PULSAR SCIENTIFIC, LLC

FDA Device Registration & Listing · Ludlow, MA, US · Registration 3010256111

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
3010256111
FEI Number
3010256111
Entity Name
PULSAR SCIENTIFIC, LLC
City/State/Country
Ludlow, MA, US
Establishment Address
8 Stony Brook St, Ludlow, MA 01056, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Pulsar Scientific, LLC (Owner Number: 10081867)
Owner / Operator Contact Address
2900 N Highway A1A, 8A, Hutchinson Island, FL 34949, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K203310
PMA Number
N/A

All Registered Proprietary Names

Pulsar Flow

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOW Sleeve, Limb, Compressible Cardiovascular Class 2 870.5800 2026-05-01

Official Correspondent

Fernando Ubidia

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Pulsar Scientific, 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 3010256111. Last updated year: 2026. Please use registration number 3010256111 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.