TRI-TECH MEDICAL, INC.

FDA Device Registration & Listing · AVON, OH, US · Registration 1530881

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
1530881
FEI Number
3002297841
Entity Name
TRI-TECH MEDICAL, INC.
City/State/Country
AVON, OH, US
Establishment Address
35401 AVON COMMERCE PARKWAY, AVON, OH 44011, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
TRI-TECH MEDICAL, INC. (Owner Number: 9034072)
Owner / Operator Contact Address
35401 AVON COMMERCE PARKWAY, --, Avon, OH 44011, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tri-Tech Medical Flowmeter Suction Bottle and Safety Trap Suction Regulator Reusable Humidifier

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAX Flowmeter, Tube, Thorpe, Back-Pressure Compensated Anesthesiology Class 1 868.2340 2021-10-12
KDQ Bottle, Collection, Vacuum General Hospital Class 2 880.6740 2020-04-14
KDP Regulator, Vacuum General Hospital Class 2 880.6740 2020-04-14
KFZ Humidifier, Non-Direct Patient Interface (Home-Use) Anesthesiology Class 1 868.5460 2020-12-21

Official Correspondent

SUNIL PARIKH

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TRI-TECH MEDICAL, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1530881. Last updated year: 2026. Please use registration number 1530881 when referencing this establishment in official correspondence.
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