TECH MEDICAL SERVICES, INC.

FDA Device Registration & Listing · Nixa, MO, US · Registration 3001003398

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
3001003398
FEI Number
3001003398
Entity Name
TECH MEDICAL SERVICES, INC.
City/State/Country
Nixa, MO, US
Establishment Address
1110 N Gerald St, Nixa, MO 65714, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Tech Medical Services, Inc. (Owner Number: 10031700)
Owner / Operator Contact Address
1450 W Jackson St. #261, Ozark, MO 65721, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Tech-Medical Services Tech-Medical Services Tech-Medical Services Tech-Medical Suction Irrigation Pump Tech-Medical Distributor/Tech Medical Services Veress Needle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KKX Drape, Surgical, Antimicrobial General, Plastic Surgery Class 2 878.4370 2019-02-11
NKC Tubing/Tubing With Filter, Insufflation, Laparoscopic Obstetrics/Gynecology Class 1 884.1730 2010-03-01
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2014-03-04
FCZ Tube, Smoke Removal, Endoscopic Gastroenterology, Urology Class 1 876.1500 2011-05-02
KZD Infusor, Pressure, For I.V. Bags General Hospital Class 1 880.5420 2011-05-02
GCJ Laparoscope, General & Plastic Surgery Gastroenterology, Urology Class 2 876.1500 2011-04-11
GCJ Laparoscope, General & Plastic Surgery Gastroenterology, Urology Class 2 876.1500 2020-02-27
FHO Pneumoperitoneum Needle Gastroenterology, Urology Class 2 876.1500 2020-03-02
HIF Insufflator, Laparoscopic Obstetrics/Gynecology Class 2 884.1730 2020-03-02

Official Correspondent

Kimberly Starks

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tech Medical Services, 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
K914369 Deroyal Industries, Inc. QUALTEX MAGNETIC INSTRUMENT DRAPE 1991-12-02
K812809 Abco Dealers, Inc. STERILE ADHERENT DRAPES 1981-11-06
K910084 Biocor Medical, Inc. SURGICAL DRAPE 1991-03-19
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826
Z-0027-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Lap Banding Kit, REF: K0398 Contains: (2) C0Q04, 5x100mm Threaded Kii Access System (1) C0604, 15x100mm Non-Threaded Separator System w/Universal Seal, for laparoscopic procedures.
Z-0028-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Lap Banding Kit, REF: K0406 Contains: (1) C0658, 11x100mm Threaded Shielded Trocar w/Universal Seal (1) C0522, 5x100mm Threaded Premium Flat Blade (1) C2202, 150mm Insufflation needle (1) C0605, 15x100mm Threaded Separator Access System (1) CB030, 5mm x 35cm Direct Drive Disposable Scissors (2) C4120, 5mm x 38cm Direct Drive Grasper Reposable Cartridge, for laparoscopic procedures.
Z-0029-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Lap Roux-EN-Y Kit, REF: K2129 Contains: (1) C0Q04, 5x100mm Threaded Kii Access System (1) C0130, 12x100mm Optical Separator System, Non-handled (2) C0Q10, 5x100mm Threaded Kii Cannula and Seal (1) C0605, 15mmx100mm Threaded Cannula System, for laparoscopic procedures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001003398. Last updated year: 2026. Please use registration number 3001003398 when referencing this establishment in official correspondence.
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