Viant San Antonio, Inc.

FDA Device Registration & Listing · San Antonio, TX, US · Registration 3013404959

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
3013404959
FEI Number
3003640911
Entity Name
Viant San Antonio, Inc.
City/State/Country
San Antonio, TX, US
Establishment Address
7027 Fairgrounds Pkwy, San Antonio, TX 78238, US
Establishment Type(s)
Manufacture Medical Device
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

TRIMANO® Drape Raphael 25 - OTS Medical OrthAlign Plus - OPU-08 K-WIRE SNIPPERS QuickPass Tendon Shuttle, Small/Large TELIGEN Port Adjuster Versys Hip System - Calcar Resection Guide Size 13,15,17 STK HRS Drop Rod - FTW Surgimedics Surgifresh Smoke Evacuator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BWN Table And Attachments, Operating-Room General, Plastic Surgery Class 1 878.4950 2022-03-04
FMF Syringe, Piston General Hospital Class 2 880.5860 2021-05-10
KQZ Component, Traction, Non-Invasive Orthopedic Class 1 888.5890 2018-10-24
NBH Accessories, Arthroscopic Orthopedic Class 1 888.1100 2018-10-24
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2018-10-24
HST Apparatus, Traction, Non-Powered Orthopedic Class 1 888.5850 2018-10-24
GAZ Tubing, Noninvasive General Hospital Class 2 880.6740 2018-10-24
MBI Fastener, Fixation, Nondegradable, Soft Tissue Orthopedic Class 2 888.3040 2026-03-23
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2026-03-25
HRX Arthroscope Orthopedic Class 2 888.1100 2018-10-24
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2016-09-15
FZG Apparatus, Air Handling, Bench General, Plastic Surgery Class 2 878.5070 2024-12-09

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
K812396 Northwest Surgical Concepts, Inc. ARTHRO-PREP REST 1981-11-20
K880350 Honway International Co. YUE/FA DISPOSABLE SYRINGE 1988-02-16
K003571 Terumo Medical Corp. SERONO FOR USE WITH GONAL-F 1200IU MULTI-DOSE ONLY AT 600IU/ML SYRINGE 2001-02-12
K083258 Dornier Medtech America, Inc. MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE 2009-01-30
K201111 Candela Corporation GentleMax Pro Plus 2020-05-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-04 Liberty Medical Supplies 2
Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 30G X 5/16'' syringes
Z-0004-04 Liberty Medical Supplies 2
Liberty brand Insulin Syringes for use with U-100 insulin, 1 cc X 29G X 1/2 '' insulin syringes
Z-0005-04 Liberty Medical Supplies 2
Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 29G X 1/2 '' insulin syringes
Z-0005-2024 Fresenius Medical Care Holdings, Inc. 2
10ML SYRINGE LUER LOCK W/OUT NEEDLE, Part Number 15-R010-0, 100 per box, 12 boxes to a case
Z-0006-2024 Fresenius Medical Care Holdings, Inc. 2
10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013404959. Last updated year: 2026. Please use registration number 3013404959 when referencing this establishment in official correspondence.
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