Viant Upland, Inc

FDA Device Registration & Listing · UPLAND, CA, US · Registration 2027487

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
2027487
FEI Number
2027487
Entity Name
Viant Upland, Inc
City/State/Country
UPLAND, CA, US
Establishment Address
2052 WEST 11TH ST., UPLAND, CA 91786, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Viant Medical, LLC (Owner Number: 9043339)
Owner / Operator Contact Address
2 Hampshire Street, Suite 202, Foxborough, MA 02035, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VELYS Patient Tracker Kit EZ-IO Needle (Non-Sterile) Mini Glenoid Baseplate 10 Degree Central Hole Drill Gauge Depth Gauge Long Depth Gauge Short Depth Gage, Adjustable Assembly Mini Glenoid Baseplate Central Depth Gauge Medtronic Depth Gauge Screw Gauge Depth Gauge Assembly, Volt System DEPTH GAGE, 2MM SCREW Biomet Depth Gauge Stryker Height Gauge Tower - ARS10247 Inferior/Superior Drill and Screw Guide Double Ended Drill Guide, 1.5/2mm Mini Baseplate Drill Guide Tip Taper Mini Baseplate Drill Guide Taper Screw Gryphon X Drill Guide - Reusable - UPL Drill Guides VOLT System STK HRS Saw Guide - FTW 2.4MM A/O DRIVE X-LOCK BLADE Revolution Radial Head

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2025-03-14
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2019-08-23
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2025-04-14
HTJ Gauge, Depth Orthopedic Class 1 888.4300 2018-12-13
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2018-12-11
FZX Guide, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2018-12-11
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2018-12-11
HXX Screwdriver Orthopedic Class 1 888.4540 2018-12-11
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2018-12-11
KWI Prosthesis, Elbow, Hemi-, Radial, Polymer Orthopedic Class 2 888.3170 2020-06-23
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2018-12-11

Official Correspondent

David Rose

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Viant Medical, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2954750 Viant Fremont, Inc FREMONT, CA, US
2244012 Viant Medical, Inc S Plainfield, NJ, US
3006194679 Viant Medical SUZHOU EPZ Co., Ltd JIANGSU PROVINCE, CN
3009493875 Viant Medical, Inc. Grand Rapids, MI, US
1832228 Viant AS&O Holdings, LLC Indianapolis, IN, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K260601 Blue Belt Technologies, Inc. REAL INTELLIGENCE™ CORI™ 2026-03-26
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09
K895079 Buckman Co., Inc. ACE BEADED K-WIRES ACE OLIVE WIRES 1989-09-13
K922193 Osteo AG OSTEO KIRSCHNER WIRE 1992-07-23
K850026 Kirkstil Corp., Inc. ORTHOPEDIC IMPLANT NAILS & PINS 1985-05-20

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
Z-0002-2022 Bard Peripheral Vascular Inc 2
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796
Z-0013-05 Biomet, Inc. 2
Lactosorb pin, 2.0 x 20 mm, sterile; ref. 948205.
Z-0005-2023 Wright Medical Technology, Inc. 2
stryker EVOLVE, Proline Stem, CoCr, Size: +2, O: 705mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radial head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.
Z-0006-2023 Wright Medical Technology, Inc. 2
stryker EVOLVE, Proline Stem, CoCr, Size: +4, OD: 9.5mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radial head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2027487. Last updated year: 2026. Please use registration number 2027487 when referencing this establishment in official correspondence.
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