Inari Medical, Costa Rica S.A.

FDA Device Registration & Listing · Grecia Alajuela, CR · Registration 3040801290

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
3040801290
FEI Number
3040801290
Entity Name
Inari Medical, Costa Rica S.A.
City/State/Country
Grecia Alajuela, CR
Establishment Address
Evolution Free Zone, Building 02, Tacares, Grecia Alajuela 20305, CR
Establishment Type(s)
Manufacture Medical Device
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
K213402
PMA Number
N/A

All Registered Proprietary Names

Large Bore Syringe, 60 cc, 3-Pack Triever Catheters Triever24 FlowTriever Retrieval/Aspiration System Large Bore Syringe, 60 cc Triever20

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KRA Catheter, Continuous Flush Cardiovascular Class 2 870.1210 2025-03-10
QEW Peripheral Mechanical Thrombectomy With Aspiration Cardiovascular Class 2 870.5150 2025-03-10

Official Correspondent

No official correspondent registered.

US Agent Details

Jayme Yamaguchi-Owens Email: jayme.yamaguchiowens@stryker.com Phone: (714) 4159129

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
2031049 TMJ Solutions, LLC San Buenaventura, CA, US
3016573902 Ortho-Space Ltd. Caesarea Haifa, IL
3010411911 POM Medical, LLC Moorpark, CA, US
8010153 BERCHTOLD GMBH & CO. KG TUTTLINGEN Baden-Wurttemberg, DE

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K792141 Pharmaseal Div., Baxter Healthcare Corp. CONTINUOUS FLUSH DEVICE 1979-12-05
K924661 Baxter Healthcare Corp SWAN-GANZ INTELLICATH CCO THERMODILUTION CATHETER 1993-04-08
K241362 Surmodics,Inc. Pounce XL Thrombectomy System (PTS-1011-7F135) 2024-09-11
K220887 Inari Medical Mini-ClotTriever Thrombectomy System 2022-08-04
K250421 Inari Medical, Inc. InThrill™ Thrombectomy System 2025-05-12

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Registration Number Establishment Name Location
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3026567963 ENDOVASCULAR ENGINEERING, INC. Menlo Park, CA, US
3021067373 VVT MED Ltd Kfar Saba Central, IL
3019525998 VASCUPATENT MEDICAL (SHENZHEN) CO., LTD Shenzhen Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040801290. Last updated year: 2026. Please use registration number 3040801290 when referencing this establishment in official correspondence.
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