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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 16 of 257
DeviceModel / ReferenceRegistriesClassStatus
Elmed ST230567
FDA UDI
Class IActive
Elmed Incorporated 32-18-03-IM
FDA UDI
Class IActive
Elmed 5703-05
FDA UDI
Class IIActive
Elmed Incorporated ST3219403IV
FDA UDI
Class IActive
Elmed EL-GL25
FDA UDI
Class IActive
Elmed Incorporated ST1717035
FDA UDI
Class IActive
Elmed Incorporated ST52205522
FDA UDI
Class IIActive
Elmed 18-3530
FDA UDI
Class IActive
Elmed 15090-60*
FDA UDI
Class IActive
Elmed 51-28260-7
FDA UDI
Class IIActive
Elmed 52236-37A
FDA UDI
Class IIActive
Elmed Incorporated ST3221901E
FDA UDI
Class IActive
Elmed 5881-09
FDA UDI
Class IIActive
Elmed ST181026
FDA UDI
Class IActive
Elmed 52105-27-18
FDA UDI
Class IIActive
Elmed ST125906I
FDA UDI
Class IIActive
Elmed Incorporated 52470-03
FDA UDI
Class IActive
Elmed 52236-129B
FDA UDI
Class IIActive
Elmed 33478-96
FDA UDI
Class IActive
Elmed Incorporated ST5225544I
FDA UDI
Class IIActive
Elmed Incorporated ST321112EV
FDA UDI
Class IActive
Elmed Incorported 32-19-402-I
FDA UDI
Class IActive
Elmed Incorporated 11-516
FDA UDI
Class IActive
Elmed Incorporated 30036-70
FDA UDI
Class IActive
Elmed Incorporated ST5215526I
FDA UDI
Class IIActive
Elmed Incorporated ST231296
FDA UDI
Class IActive
Elmed 13-70-08
FDA UDI
Class IActive
Elmed Incorporated R42-3040
FDA UDI
Class IActive
Elmed ST2380002
FDA UDI
Class IActive
Elmed 41452-03
FDA UDI
Class IActive
Elmed ST243785135
FDA UDI
Class IActive
Elmed ST0942517
FDA UDI
Class IActive
Elmed 32-10-13A-I
FDA UDI
Class IActive
Elmed 52224-11C
FDA UDI
Class IIActive
Elmed ST3341525
FDA UDI
Class IActive
Elmed Incorporated 5211-08*
FDA UDI
Class IActive
Elmed Incorporated 31540-61
FDA UDI
Class IActive
Elmed Incorporated ST52255156I
FDA UDI
Class IIActive
Elmed Incorporated ST5255547
FDA UDI
Class IIActive
Elmed Incorporated ST321013EM
FDA UDI
Class IActive
Elmed Incorporated ST124315
FDA UDI
Class IActive
Elmed Incorporated ST5200100
FDA UDI
Class IIActive
Elmed Incorporated ST3261025
FDA UDI
Class IIActive
Elmed 24129-25
FDA UDI
Class IActive
Elmed 23-80002
FDA UDI
Class IActive
Elmed Incorporated ST5210321I
FDA UDI
Class IIActive
Elmed 32-25-01-E
FDA UDI
Class IActive
Elmed 54050-07
FDA UDI
Class IIActive
Elmed 24-0803CC-FU
FDA UDI
Class IActive
Elmed 52208-113
FDA UDI
Class IIActive

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