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Techcord co., Ltd

US

Last updated May 24, 2026

What Techcord co., Ltd makes

Techcord co., Ltd manufactures single-use arthroscopic shaver system blades designed for surgical procedures. These blades are intended for use in arthroscopic surgeries to remove tissue or debris from joints, improving precision and efficiency during minimally invasive procedures.

The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Techcord co., Ltd manufacture?

Techcord co., Ltd specializes in single-use arthroscopic shaver system blades. These devices are specifically designed for arthroscopic surgeries, where they help remove tissue or debris from joints during minimally invasive procedures. The focus is on precision and efficiency in surgical applications.

Where is Techcord co., Ltd based?

Techcord co., Ltd is headquartered in the United States. The company’s location is relevant for understanding its regulatory environment and operational reach, particularly in relation to FDA compliance and reporting requirements.

Which regulatory registries list Techcord co., Ltd’s devices?

Techcord co., Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, distributors, and regulatory authorities, allowing them to verify device details and compliance status.

How are Techcord co., Ltd’s devices classified under medical device regulations?

Techcord co., Ltd’s arthroscopic shaver system blades fall under the FDA’s Class I medical device classification. This classification is typically assigned to devices posing the lowest risk to patients, often involving minimal or non-invasive procedures. Class I devices generally require less stringent regulatory oversight compared to higher-risk categories.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+82422210015
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
688890630

Catalogue (106)

Page 2 of 3
DeviceModel / ReferenceRegistriesClassStatus
SharkCut TSL1930D
FDA UDI
Class IActive
SharkCut TSS2840C
FDA UDI
Class IActive
SharkCut T1742
FDA UDI
Class IActive
SharkCut T3930
FDA UDI
Class IActive
SharkCut T2655
FDA UDI
Class IActive
SharkCut TSN3530D
FDA UDI
Class IActive
SharkCut T3942
FDA UDI
Class IActive
SharkCut T1750
FDA UDI
Class IActive
SharkCut T2730
FDA UDI
Class IActive
SharkCut TSS2830C
FDA UDI
Class IActive
SharkCut TSN1940D
FDA UDI
Class IActive
SharkCut T1930
FDA UDI
Class IActive
SharkCut T1855
FDA UDI
Class IActive
SharkCut T1830
FDA UDI
Class IActive
SharkCut T1635
FDA UDI
Class IActive
SharkCut T1655
FDA UDI
Class IActive
SharkCut T2830
FDA UDI
Class IActive
SharkCut TSS2850D
FDA UDI
Class IActive
SharkCut RB2840
FDA UDI
Class IActive
SharkCut RB2730
FDA UDI
Class IActive
SharkCut T1942
FDA UDI
Class IActive
SharkCut T1950
FDA UDI
Class IActive
SharkCut T2742
FDA UDI
Class IActive
SharkCut TSL3530C
FDA UDI
Class IActive
SharkCut TSL2840D
FDA UDI
Class IActive
SharkCut T1842
FDA UDI
Class IActive
SharkCut T2850
FDA UDI
Class IActive
SharkCut T3750
FDA UDI
Class IActive
SharkCut RB2850
FDA UDI
Class IActive
SharkCut T1935
FDA UDI
Class IActive
SharkCut T2955
FDA UDI
Class IActive
SharkCut TSN2840C
FDA UDI
Class IActive
SharkCut T2755
FDA UDI
Class IActive
SharkCut OB1940
FDA UDI
Class IActive
SharkCut TSS2840D
FDA UDI
Class IActive
SharkCut T1850
FDA UDI
Class IActive
SharkCut T2635
FDA UDI
Class IActive
SharkCut T3935
FDA UDI
Class IActive
SharkCut RB2640
FDA UDI
Class IActive
SharkCut OB1850
FDA UDI
Class IActive
SharkCut RB2740
FDA UDI
Class IActive
SharkCut TSN1930D
FDA UDI
Class IActive
SharkCut T3742
FDA UDI
Class IActive
SharkCut T3730
FDA UDI
Class IActive
SharkCut RB2950
FDA UDI
Class IActive
SharkCut T3642
FDA UDI
Class IActive
SharkCut T3635
FDA UDI
Class IActive
SharkCut TSS3530C
FDA UDI
Class IActive
SharkCut RB2940
FDA UDI
Class IActive
SharkCut T1642
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Techcord Co., Ltd. Daejeon · KR FEI 3026090987