MISSION SURGICAL INNOVATIONS

FDA Device Registration & Listing · Raleigh, NC, US · Registration 3013450929

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
3013450929
FEI Number
3013450929
Entity Name
MISSION SURGICAL INNOVATIONS
City/State/Country
Raleigh, NC, US
Establishment Address
7424 Acc Blvd, Suite 104, Raleigh, NC 27617, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Mission Surgical Innovations (Owner Number: 10054060)
Owner / Operator Contact Address
7424 Acc Blvd, Suite 104, Raleigh, NC 27617, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SafeView ClearGuard LE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2017-02-07

Official Correspondent

Brian Garvey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mission Surgical Innovations
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0009-2007 Smith & Nephew Inc 1
Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007 Smith & Nephew Inc 1
Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06 Stryker Howmedica Osteonics Corp. 1
Allocraft TLIF Bone Inserter.
Z-0011-2007 Smith & Nephew Inc 1
Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011 Depuy Orthopaedics, Inc. 1
Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

Similar Registrations

Registration Number Establishment Name Location
3018033084 NEXT GENERATION TOOLING INC Akron, OH, US
3038207124 NATIVE ORTHOPAEDICS Providence, RI, US
3027516563 STAR SPORTS MEDICINE CO., LTD. Beijing, CN
3021574846 3D LOGICS LLC Hillsboro, OR, US
3030089866 ORTOLOG MEDIKAL SANAYI VE TICARET A.S. Yenimahalle Ankara, TR
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013450929. Last updated year: 2026. Please use registration number 3013450929 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.