Data / Medical devices / United States / Tech Medical Services, Inc.

Tech Medical Services, Inc.: FDA-registered device maker in Nixa, MO, United States, 6 510(k) clearances

Name: Tech Medical Services, Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Tech Medical Services, Inc. is registered with the FDA (registration 3001003398) in Nixa, MO, United States. It lists 10 device types. The FDA files 6 510(k) clearances under its listings, the newest dated December 20, 2011. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3001003398
Address: 1110 N Gerald St, Nixa, MO, United States, 65714
Owner or operator: Tech Medical Services, Inc. (10031700)
Roles: Repackager or relabeler, Specification developer
First device listed: March 1, 2010
Registered through: 2026
Brand names listed: Distributor/Tech Medical Services, Endo Pouches, Suction Irrigation Pump, Tech-Medical, Tech-Medical Services, Veress Needle

Devices it lists

Device	Product code	Class	Role	Source
Drape, Surgical, Antimicrobial	KKX	2	Repackager or relabeler	accessdata.fda.gov
Electrosurgical, Cutting & Coagulation & Accessories	GEI	2	Repackager or relabeler	accessdata.fda.gov
Guide, Needle, Surgical	GDF	1	Repackager or relabeler	accessdata.fda.gov
Infusor, Pressure, For I.V. Bags	KZD	1	Repackager or relabeler	accessdata.fda.gov
Insufflator, Laparoscopic	HIF	2	Repackager or relabeler	accessdata.fda.gov
Laparoscope, General & Plastic Surgery	GCJ	2	Repackager or relabeler	accessdata.fda.gov
Laparoscopic Accessories, Gynecologic	NWV	1	Repackager or relabeler, Specification developer	accessdata.fda.gov
Pneumoperitoneum Needle	FHO	2	Repackager or relabeler	accessdata.fda.gov
Tube, Smoke Removal, Endoscopic	FCZ	1	Repackager or relabeler	accessdata.fda.gov
Tubing/Tubing With Filter, Insufflation, Laparoscopic	NKC	1	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
December 20, 2011	K103508	UNMIAX LAPAROSCOPIC INSTRUMENT	GEI	Substantially Equivalent	Unimax Medical Systems, Inc.	accessdata.fda.gov
August 19, 2011	K111441	UNIMAX VERESS NEEDLE	HIF	Substantially Equivalent	Unimax Medical Systems, Inc.	accessdata.fda.gov
May 19, 2011	K103509	UNIMAX SUCTION IRRIGATION SET	GCJ	Substantially Equivalent	Unimax Medical Systems, Inc.	accessdata.fda.gov
May 6, 2011	K103510	UNIMAX SPECIMEN RETRIEVAL SYSTEM	GCJ	Substantially Equivalent	Unimax Medical Systems, Inc.	accessdata.fda.gov
November 12, 2004	K041967	GENICON SUCTION IRRIGATION SYSTEM	GCJ	Substantially Equivalent	Genicon	accessdata.fda.gov
October 28, 1994	K934630	UNIVERSAL VIDEO/LASER ARM DRAPE	KKX	Substantially Equivalent	Hydro-Med Products, Inc.	accessdata.fda.gov

Compare with other makers

Updated December 20, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.