LimFlow Inc.

FDA Device Registration & Listing · Irvine, CA, US · Registration 3023527320

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
3023527320
FEI Number
3023527320
Entity Name
LimFlow Inc.
City/State/Country
Irvine, CA, US
Establishment Address
6001 Oak Canyon, Suite 100, Irvine, CA 92618, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
STRYKER CORP. (Owner Number: 1811755)
Owner / Operator Contact Address
4100 East Milham Ave., Kalamazoo, MI 49001, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K251376
PMA Number
N/A

All Registered Proprietary Names

LimFlow Extension Stent Graft LimFlow System LimFlow Crossing Stent Graft LimFlow Vector LimFlow ARC LimFlow V-Ceiver LimFlow ARC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QWN Stent Graft, Infrapopliteal, Venous Arterialization Unknown Class 3 N/A 2025-03-17
MGZ Valvulotome Cardiovascular Class 2 870.4885 2026-04-13
PDU Catheter For Crossing Total Occlusions Cardiovascular Class 2 870.1250 2025-03-17
MMX Device, Percutaneous Retrieval Cardiovascular Class 2 870.5150 2025-03-17
PDU Catheter For Crossing Total Occlusions Cardiovascular Class 2 870.1250 2025-06-03

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

STRYKER CORP.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3003897776 BIOMIMETIC THERAPEUTICS,LLC FRANKLIN, TN, US
3040801290 Inari Medical, Costa Rica S.A. Grecia Alajuela, CR
2031049 TMJ Solutions, LLC San Buenaventura, CA, US
3016573902 Ortho-Space Ltd. Caesarea Haifa, IL
3010411911 POM Medical, LLC Moorpark, CA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K071227 Spectranetics Corp. CLIRPATH TURBO EXCIMER LASER CATHETER (RX) -0.9MM, (RX) -1.4MM, (RX) -1.7MM, (RX) -2.0MM, MODEL 310-154, 314-159, 317-15 2007-07-11
K213494 ABBOTT MEDICAL Aveir Retrieval Catheter 2022-04-01

Similar Registrations

Registration Number Establishment Name Location
3009018440 Nitinol Devices & Components Costa Rica, S. R. L. El Coyol Alajuela, CR
3010273872 Synergy Health AST, SRL Alajuela, CR
3009039068 HA2 MEDIZINTECHNIK GMBH Halberstadt Saxony-Anhalt, DE
3003637635 Contract Medical International GmbH DRESDEN Saxony, DE
1319639 Sterigenics U.S., LLC Queensbury, NY, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023527320. Last updated year: 2026. Please use registration number 3023527320 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.