CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.)

FDA Device Registration & Listing · Morgan Hill, CA, US · Registration 3009906207

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
3009906207
FEI Number
3009906207
Entity Name
CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.)
City/State/Country
Morgan Hill, CA, US
Establishment Address
18705 Madrone Pkwy, Suite 150, Morgan Hill, CA 95037, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Cordica Medical (Formally Team Technologies, Inc) (Owner Number: 1051594)
Owner / Operator Contact Address
5949 COMMERCE BLVD., --, Morristown, TN 37814, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

T.Ox

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MUD Oximeter, Tissue Saturation Cardiovascular Class 2 870.2700 2025-12-26

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cordica Medical (Formally Team Technologies, Inc)
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3007125968 CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.) Chino, CA, US
3015807001 CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.) Sunrise, FL, US
3006187135 CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.) BATAVIA, IL, US
3004713654 CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.) Haverhill, MA, US
1933975 CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.) Earth City, MO, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K201432 Masimo Corporation Masimo O3 Regional Oximeter System 2020-08-29
K211561 Covidien, LLC INVOS PM7100 Patient Monitor, INVOS Pediatric rSO2 Sensor, INVOS Infant Regional Saturation Sensor (also referred to as OxyAlert NIRSensor) 2021-12-05

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009906207. Last updated year: 2026. Please use registration number 3009906207 when referencing this establishment in official correspondence.
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