Mass Precision, Inc.

FDA Device Registration & Listing · Fremont, CA, US · Registration 3014309390

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
3014309390
FEI Number
3014309390
Entity Name
Mass Precision, Inc.
City/State/Country
Fremont, CA, US
Establishment Address
46555 Landing Parkway, Fremont, CA 94538, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
Mass Precision, Inc. (Owner Number: 10081926)
Owner / Operator Contact Address
2110 Oakland Road, San Jose, CA 95131, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SRK, English, IS4000 IRK,OUS,W/O VS,IS4000 IRK,OUS,W/O VS,IS3000 IRK,OUS,IS4000 IRK,OUS,IS3000 Kit, IRK, Endowrist Instruments, IS1200/2000/3000 SRK,OUS,IS4000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAY System, Surgical, Computer Controlled Instrument Gastroenterology, Urology Class 2 876.1500 2021-05-26
GDW Staple, Implantable General, Plastic Surgery Class 2 878.4750 2021-05-26
NAY System, Surgical, Computer Controlled Instrument Gastroenterology, Urology Class 2 876.1500 2022-01-19
NAY System, Surgical, Computer Controlled Instrument Gastroenterology, Urology Class 2 876.1500 2021-05-26
GDW Staple, Implantable General, Plastic Surgery Class 2 878.4750 2022-01-19

Official Correspondent

Matthew Stucky

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mass Precision, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K131563 Opus Ksd, Inc. SUBQ IT! BIOABSORBABLE SKIN CLOSURE SYSTEM 2014-04-09
K131705 Covidien, Formerly US Surgical A Divison of Tyco H ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY 2013-07-01
K103263 Covidien, Formerly US Surgical A Divison of Tyco H ENDO GIA SINGLEUSE DUET TRS RELOAD WITH TRI0STAPLE TECHNOLOGY 2010-11-22
K130717 Covidien, Formerly US Surgical A Divison of Tyco H ENDO GIA RELOAD 2013-04-18
K221006 Covidien GIA Stapler with Tri-Staple Technology 2022-04-29

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2021 N/A 2
Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm, Item Code 030450 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Z-0002-2021 N/A 2
Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm, Item Code 030451 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Z-0003-2021 N/A 2
Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm, Item Code 030452 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Z-0004-2021 N/A 2
Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm, Item Code 030453 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Z-0005-2021 N/A 2
Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm, Item Code 030454 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014309390. Last updated year: 2026. Please use registration number 3014309390 when referencing this establishment in official correspondence.
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