Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009266751

FEI Number

3009266751

Entity Name

Cadence Inc.

City/State/Country

Staunton, VA, US

Establishment Address

9 Technology Dr, Staunton, VA 24401, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Cadence, Inc. (Owner Number: 2414164)

Owner / Operator Contact Address

9 Technology Drive, Staunton, VA 24401, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GFA	Blade, Saw, General & Plastic Surgery, Surgical	General, Plastic Surgery	Class 1	878.4820	2012-12-13
DWH	Blade, Saw, Surgical, Cardiovascular	General, Plastic Surgery	Class 1	878.4820	2012-12-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cadence, 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
1213649	Cadence Science, Inc.	Cranston, RI, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K953012	Boston Surgical Products, Inc.	DISPOSABLE & REUSABLE SURGICAL CUTTING TOOLS	1995-07-12

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3027344440	TRITEX MEDICAL MANUFACTURING LLC	Mount Morris, MI, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009266751. Last updated year: 2026. Please use registration number 3009266751 when referencing this establishment in official correspondence.