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ELMED INCORPORATED

US

Last updated May 24, 2026

What ELMED INCORPORATED makes

Elmed Incorporated manufactures reusable surgical instruments, including rigid endoscopic forceps for tissue manipulation, laparoscopes, and laparoscopic surgical procedure kits. Their portfolio also covers reusable hand-held retractors, bipolar and monopolar electrosurgical handpieces and electrodes for open-surgery, as well as non-medicated ENT and arthroscopic surgical procedure kits.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Elmed Incorporated is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Elmed Incorporated manufacture?

Elmed Incorporated specializes in reusable surgical instruments, including rigid endoscopic tissue manipulation forceps, laparoscopes, and laparoscopic surgical procedure kits. Their product range also includes reusable hand-held retractors, bipolar and monopolar electrosurgical handpieces/electrodes for open-surgery, as well as non-medicated ENT and arthroscopic surgical procedure kits. These devices are designed for various surgical applications, from minimally invasive procedures to open surgeries.

Where is Elmed Incorporated based?

Elmed Incorporated is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution, particularly for FDA-related processes.

Which regulatory registries list Elmed Incorporated’s devices?

Elmed Incorporated’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their lifecycle, ensuring transparency and traceability in regulatory and clinical settings.

How are Elmed Incorporated’s devices classified under FDA regulations?

Elmed Incorporated’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose the lowest risk and may require less regulatory oversight, while Class II devices involve moderate risk and typically require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway and requirements for each device.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
elmed.com
LinkedIn
—
Facebook
—
Phone
224-353-6446
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
049290364

Catalogue (12842)

Page 25 of 257
DeviceModel / ReferenceRegistriesClassStatus
Elmed 5950-06
FDA UDI
Class IIActive
Elmed 23-5010-03
FDA UDI
Class IActive
Elmed 5-0536-53A
FDA UDI
Class IIActive
Elmed 32-10-13
FDA UDI
Class IActive
Elmed 18-3790
FDA UDI
Class IActive
Elmed 5-0545-122A
FDA UDI
Class IIActive
Elmed Incorporated 30-643-03F
FDA UDI
Class IActive
Elmed ST31002
FDA UDI
Class IActive
Elmed EL-GL500
FDA UDI
Class IActive
Elmed Incorporated ST7141026
FDA UDI
Class IActive
Elmed 09161-14
FDA UDI
Class IActive
Elmed Incorporated ST5250220B
FDA UDI
Class IIActive
Elmed ST124600I
FDA UDI
Class IIActive
Elmed Incorporated 01-3360
FDA UDI
Class IActive
Elmed Incorporated ST52155160I
FDA UDI
Class IIActive
Elmed Incorporated 23-869051
FDA UDI
Class IActive
Elmed Incorporated ST3216018E
FDA UDI
Class IActive
Elmed 52626-41C
FDA UDI
Class IIActive
Elmed 5913-08
FDA UDI
Class IIActive
Elmed 31-005*
FDA UDI
Class IActive
Elmed Incorporated 40-2588
FDA UDI
Class IActive
Elmed Incorporated ST241502
FDA UDI
Class IActive
Elmed Incorporated ST23TKBAR
FDA UDI
Class IActive
Elmed 52224-136B
FDA UDI
Class IIActive
Elmed 5322-07
FDA UDI
Class IIActive
Elmed 5-0545-69A
FDA UDI
Class IIActive
Elmed 5-0536-61A
FDA UDI
Class IIActive
Elmed 15040-6231
FDA UDI
Class IActive
Elmed 52265-77A
FDA UDI
Class IIActive
Elmed ST1230624
FDA UDI
Class IActive
Elmed ST13900GL
FDA UDI
Class IActive
Elmed 36-410121
FDA UDI
Class IActive
Elmed 33668-12C
FDA UDI
Class IActive
Elmed Incorporated ST321003IV
FDA UDI
Class IUnknown
Elmed 52224-48B
FDA UDI
Class IIActive
Elmed 52155-41C
FDA UDI
Class IIActive
Elmed E5950-08
FDA UDI
Class IIActive
Elmed 53020-60C
FDA UDI
Class IIActive
Elmed 52832-443
FDA UDI
Class IIActive
Elmed 5623-05
FDA UDI
Class IIActive
Elmed Incorporated ST52224122I
FDA UDI
Class IIActive
Elmed 5860-06C
FDA UDI
Class IIActive
Elmed 5730-08
FDA UDI
Class IIActive
Elmed Incorporated 52501-07B
FDA UDI
Class IIActive
Elmed Incorporated ST3219411IM
FDA UDI
Class IActive
Elmed Incorporated STS5017750
FDA UDI
Class IActive
Elmed 52256-68
FDA UDI
Class IIActive
Elmed ST1111018
FDA UDI
Class IActive
Elmed 52224-39B
FDA UDI
Class IIActive
Elmed 52605-27B
FDA UDI
Class IIActive

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