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Tecno Instruments (Pvt.) , Ltd.

US

Last updated May 27, 2026

What Tecno Instruments (Pvt.) , Ltd. makes

Tecno Instruments (Pvt.) Ltd. manufactures reusable surgical instruments, including bipolar electrosurgical handpieces and electrodes for open-surgery procedures, vaginal speculums, self-retaining retractors, soft-tissue manipulation forceps, surgical hooks, and reusable electrical connection cables. They also produce single-use electrosurgical handpieces designed for precision tissue manipulation during surgical operations.

The company’s products are regulated under FDA classifications, with devices falling into Class I and Class II categories. These instruments are listed in the FDA’s 510(k) and UDI registries, ensuring compliance with U.S. medical device authorisation requirements. Tecno Instruments (Pvt.) Ltd. operates from 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 Tecno Instruments (Pvt.) Ltd. manufacture?

Tecno Instruments (Pvt.) Ltd. specialises in reusable surgical instruments, including bipolar electrosurgical handpieces and electrodes for open-surgery, vaginal speculums, self-retaining retractors, soft-tissue manipulation forceps, surgical hooks, and reusable electrical connection cables. They also produce single-use electrosurgical handpieces, which are designed for controlled tissue manipulation during surgical procedures. These devices are primarily used in operating rooms to assist in precision surgical tasks.

Where is Tecno Instruments (Pvt.) Ltd. based?

Tecno Instruments (Pvt.) Ltd. is headquartered in the United States. The company’s location ensures it operates within U.S. regulatory frameworks, including those governing medical device authorisation and compliance.

Which regulatory registries list Tecno Instruments’ devices?

Tecno Instruments’ devices are listed in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identification (UDI) system. These registries ensure that each device meets U.S. requirements for medical device authorisation and traceability, helping healthcare providers and regulators track compliance.

How are Tecno Instruments’ devices classified under FDA regulations?

Tecno Instruments’ devices are classified under two FDA categories: Class I and Class II. The classification depends on factors like the device’s intended use, risk level, and potential impact on patient safety. For example, reusable surgical instruments like forceps or retractors may fall into Class II due to their role in critical procedures, while lower-risk items like certain reusable cables might qualify as Class I. These classifications determine the regulatory pathway for authorisation.

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

Information

Country
US
Address
—
Website
tecno.com.pk
LinkedIn
—
Facebook
—
Phone
+92523552723
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
645519047

Catalogue (90)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
Tecno 130-119
FDA UDI
Class IActive
Tecno 110-320-10 UP
FDA UDI
Class IIActive
Tecno 130-122
FDA UDI
Class IActive
Tecno 110-340-10
FDA UDI
Class IIActive
Tecno 130-140
FDA UDI
Class IActive
Tecno 130-170
FDA UDI
Class IActive
Tecno 110-310-10
FDA UDI
Class IIActive
Tecno 110-370-15
FDA UDI
Class IIActive
Tecno 130-175
FDA UDI
Class IActive
Tecno 110-370-05
FDA UDI
Class IIActive
Tecno 130-103
FDA UDI
Class IActive
Tecno 110-430-15
FDA UDI
Class IIActive
Tecno 110-815-18
FDA UDI
Class IIActive
Tecno 110-180-10
FDA UDI
Class IIActive
Tecno 110-440-10
FDA UDI
Class IIActive
Tecno 110-100-05
FDA UDI
Class IIActive
Tecno 130-124
FDA UDI
Class IActive
Tecno 110-320-10 DN
FDA UDI
Class IIActive
Tecno 130-134
FDA UDI
Class IActive
Tecno 130-100
FDA UDI
Class IActive
Tecno 110-190-10
FDA UDI
Class IIActive
Tecno 130-181
FDA UDI
Class IActive
Tecno 130-108
FDA UDI
Class IActive
Tecno 130-182
FDA UDI
Class IActive
Tecno 130-133
FDA UDI
Class IActive
Tecno 110-300-10
FDA UDI
Class IIActive
Tecno 110-365-07
FDA UDI
Class IIActive
Tecno 130-203
FDA UDI
Class IActive
Tecno 130-185 ET
FDA UDI
Class IActive
Tecno 110-350-10
FDA UDI
Class IIActive
Tecno 110-140-05
FDA UDI
Class IIActive
Tecno 130-183
FDA UDI
Class IActive
Tecno 130-111
FDA UDI
Class IActive
Tecno 110-240-10
FDA UDI
Class IIActive
Tecno 130-186 ET
FDA UDI
Class IActive
Tecno 110-460-07
FDA UDI
Class IIActive
Tecno 110-225-15
FDA UDI
Class IIActive
Tecno 110-110-05
FDA UDI
Class IIActive
Tecno 110-230-10
FDA UDI
Class IIActive
Tecno 130-176
FDA UDI
Class IActive
Tecno 130-117
FDA UDI
Class IActive
Tecno 130-109
FDA UDI
Class IActive
Tecno 110-140-07
FDA UDI
Class IIActive
Tecno 110-360-05
FDA UDI
Class IIActive
Tecno 110-370-10
FDA UDI
Class IIActive
Tecno 110-170-05
FDA UDI
Class IIActive
Tecno 130-113
FDA UDI
Class IActive
Tecno 110-320-10
FDA UDI
Class IIActive
Tecno 130-104
FDA UDI
Class IActive
Tecno 130-202
FDA UDI
Class IActive

Related Companies

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FDA Establishments (1)

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

  • Tecno Instruments (pvt.) Ltd. SIALKOT Punjab · PK FEI 3002808325