MEDITRINA, INC.

FDA Device Registration & Listing · San Jose, CA, US · Registration 3015512350

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
3015512350
FEI Number
3015512350
Entity Name
MEDITRINA, INC.
City/State/Country
San Jose, CA, US
Establishment Address
1190 Saratoga Ave, Suite 180, San Jose, CA 95129, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Meditrina, Inc. (Owner Number: 10061575)
Owner / Operator Contact Address
1190 Saratoga Ave, Suite 180, San Jose, CA 95129, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K190372
PMA Number
N/A

All Registered Proprietary Names

Aveta Drape Pump Aveta Tissue Catch with Tubing Aveta Pearl Disposable Hysteroscope Aveta Disposable Resecting Handset Aveta Reusable Resecting Handset Aveta System Aveta Controller Aveta Roll Stand with Drape Pump Aveta Fluid Management Accessory Aveta Tissue Catch with Suction Tubing Aveta Disposable Resecting Device, 3.9mm Aveta Coral Disposable Hysteroscope Aveta Flex Disposable Resecting Device, 2.9mm Aveta Waste Bag, 6L Aveta Disposable Resecting Device, 2.9mm Aveta Waste Management Accessory Aveta Smol Disposable Resecting Device, 2.9mm Aveta Opal Reusable Cable Aveta Max+ Disposable Resecting Device, 3.9mm Aveta Auto Disposable Resecting Device Aveta Opal Disposable Hysteroscope, 4.6mm Aveta Tissue Catch Aveta Smol Disposable Resecting Tip, 2.9mm Aveta Flex+ Disposable Resecting Device, 2.9mm Aveta Wave+ Disposable Resecting Tip, 3.9mm Aveta Auto 5 Fr Disposable Resecting Device Aveta Flex Disposable Resecting Tip, 2.9mm

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HIG Insufflator, Hysteroscopic Obstetrics/Gynecology Class 2 884.1700 2019-10-30
HIH Hysteroscope (And Accessories) Obstetrics/Gynecology Class 2 884.1690 2019-10-30

Official Correspondent

Lyudmila Kokish

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Meditrina, Inc.
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
K905706 Circon Acmi GYN-1500 HYSTEROSCOPIC INUFFLATOR 1991-02-28
K935716 KARL STORZ Endoscopy-America, Inc. KARL STORZ FIXED MAGNIFICATION TELESCOPE/KS VARIABLE MAGNIFICATION TELESCOPE 1995-11-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015512350. Last updated year: 2026. Please use registration number 3015512350 when referencing this establishment in official correspondence.
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