Data / Medical devices / Pakistan / Tecno Instruments (pvt.) Ltd.
Tecno Instruments (pvt.) Ltd.: FDA-registered device maker in SIALKOT Punjab, Pakistan, 4 510(k) clearances
Tecno Instruments (pvt.) Ltd. is registered with the FDA (registration 9613563) in SIALKOT Punjab, Pakistan. It lists 11 device types. The FDA files 4 510(k) clearances under its listings, the newest dated May 3, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9613563
- FEI number
- 3002808325
- Address
- 316-C Small Industrial Estate, SIALKOT Punjab, Pakistan, 51340
- Owner or operator
- Tecno Instruments (Pvt) Ltd. (9019852)
- Roles
- Contract manufacturer, Contract sterilizer, Exporter to the US, Manufacturer
- First device listed
- April 17, 1995
- Registered through
- 2026
- Brand names listed
- Adson, Bipolar Cable, Bipolar Forceps, Callisto Greenline D / Standard D Laryngoscope Blade and Handle, Collin, Cusco, Cushing, Dressing Forceps and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Elevator, Surgical, Dental | EMJ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Forceps | HTD | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Forceps, Ophthalmic | HNR | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Hook, Surgical, General & Plastic Surgery | GDG | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Laryngoscope, Rigid | CCW | 1 | Contract sterilizer | accessdata.fda.gov |
| Pliers, Operative | EJY | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Retractor, All Types | EIG | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Retractor, Vaginal | HDL | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Speculum, Vaginal, Metal | HDF | 1 | Exporter to the US, Manufacturer | 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 |
|---|---|---|---|---|---|---|
| May 3, 2017 | K170107 | Surgi Max Ultra | GEI | Substantially Equivalent | Elliquence, LLC | accessdata.fda.gov |
| October 18, 2004 | K042608 | TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110 | GEI | Substantially Equivalent | Tecno Instruments (Pvt.) , Ltd. | accessdata.fda.gov |
| October 19, 2000 | K002257 | TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 | GEI | Substantially Equivalent | Tecno Instruments (Pvt.) , Ltd. | accessdata.fda.gov |
| August 14, 1997 | K964176 | TECNO REUSABLE, ELECTROSURGICAL, BIPOLAR FORCEPS | GEI | Substantially Equivalent | Tecno Instruments (Usa), Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Scissors, General, Surgical
- All makers of Forceps, Ophthalmic
- All makers of Forceps
- All makers of Laryngoscope, Rigid
- All makers of Pliers, Operative
Updated May 3, 2017. 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.