SEQUEL MEDICAL INC.

FDA Device Registration & Listing · Fort Lauderdale, FL, US · Registration 3017168764

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
3017168764
FEI Number
3017168764
Entity Name
SEQUEL MEDICAL INC.
City/State/Country
Fort Lauderdale, FL, US
Establishment Address
8551 W Sunrise Blvd, STE 300, Plantation, Fort Lauderdale, FL 33322, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Sequel Medical Inc (Owner Number: 10076685)
Owner / Operator Contact Address
8551 W Sunrise Blvd., Ste. 200 Plantation, Fort Lauderdale, FL 33322, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Sequel Medical Inc

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic Class 2 888.3030 2021-02-12

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sequel Medical 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
K033476 Howmedica Osteonics Corp. MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM 2004-01-20

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017168764. Last updated year: 2026. Please use registration number 3017168764 when referencing this establishment in official correspondence.
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