MICRO TYPING SYSTEMS, INC.

FDA Device Registration & Listing · POMPANO BEACH, FL, US · Registration 1056600

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
1056600
FEI Number
1000132079
Entity Name
MICRO TYPING SYSTEMS, INC.
City/State/Country
POMPANO BEACH, FL, US
Establishment Address
1295 SW 29TH AVE, POMPANO BEACH, FL 33069, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
QuidelOrtho Corporation (Owner Number: 2024674)
Owner / Operator Contact Address
9975 Summers Ridge Road, San Diego, CA 92121, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK950028
PMA Number
N/A

All Registered Proprietary Names

MTS Buffered Gel Card MTS ID Tipmaster MTS Dispenser (0.5 mL and 1 mL)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KSZ System, Test, Automated Blood Grouping And Antibody Hematology Class 2 864.9175 2022-12-21
KSS Supplies, Blood-Bank Hematology Class 1 864.9050 2022-12-21
KSS Supplies, Blood-Bank Hematology Class 1 864.9050 2022-12-21

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3002642396 Ortho Clinical Diagnostics Singapore South West, SG
2250051 ORTHO-CLINICAL DIAGNOSTICS, INC. RARITAN, NJ, US
1528450 Ortho-Clinical Diagnostics, Inc. ATHENS, OH, US
2024674 QUIDEL CORP. SAN DIEGO, CA, US
3012963943 Ortho Clinical Diagnostics, K.K. Shinagawa-ku Tokyo, JP

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1056600. Last updated year: 2026. Please use registration number 1056600 when referencing this establishment in official correspondence.
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