DePuy Synthes West Palm Beach

FDA Device Registration & Listing · West Palm Beach, FL, US · Registration 3025110439

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
3025110439
FEI Number
3025110439
Entity Name
DePuy Synthes West Palm Beach
City/State/Country
West Palm Beach, FL, US
Establishment Address
374 N Haverhill Rd Ste 400, West Palm Beach, FL 33415, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
THE ANSPACH EFFORT, INC. (Owner Number: 1045834)
Owner / Operator Contact Address
4500 Riverside Dr, Palm Beach Gardens, FL 33410, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

VELYS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2025-03-21

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

THE ANSPACH EFFORT, 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
1045834 THE ANSPACH EFFORT, INC. Palm Bch Gdns, FL, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K260601 Blue Belt Technologies, Inc. REAL INTELLIGENCE™ CORI™ 2026-03-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0041-2024 Blue Belt Technologies, Inc 2
Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025110439. Last updated year: 2026. Please use registration number 3025110439 when referencing this establishment in official correspondence.
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