Data / Medical devices / Pakistan / Sahiroun (pvt) Ltd.
Sahiroun (pvt) Ltd.: FDA-registered device maker in SIALKOT Punjab, Pakistan, 1 510(k) clearance
Sahiroun (pvt) Ltd. is registered with the FDA (registration 9613073) in SIALKOT Punjab, Pakistan. It lists 16 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 19, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9613073
- FEI number
- 3003927064
- Address
- Wazirabad Road, Rahimpur, Ugoki, SIALKOT Punjab, Pakistan, 51310
- Owner or operator
- SAHIROUN (PVT) LTD. (9022104)
- Roles
- Manufacturer
- First device listed
- August 29, 1995
- Registered through
- 2026
- Brand names listed
- CARTRIDGE SYRINGE ALL TYPES, CHEST PIECE, CUSCO, COLLIN, GRAVES, DOYEN, BALFOUR, LANGENBECK, ENDOTRACHEAL, FRAZIER, POOL, YANKAUER, GENERAL, MASTERGLIDE, ECONOGLIDE and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Forceps | HTD | 1 | Manufacturer | accessdata.fda.gov |
| Forceps, Tube Introduction | BWB | 1 | Manufacturer | accessdata.fda.gov |
| Hemostat | HRQ | 1 | Manufacturer | accessdata.fda.gov |
| Holder, Needle, Gastroenterologic | FHQ | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Surgical, Non-Powered | HAO | 1 | Manufacturer | accessdata.fda.gov |
| Laryngoscope, Rigid | CCW | 1 | Manufacturer | accessdata.fda.gov |
| Mirror, Ent | KAI | 1 | Manufacturer | accessdata.fda.gov |
| Ophthalmoscope, Battery-Powered | HLJ | 2 | Manufacturer | accessdata.fda.gov |
| Otoscope | ERA | 1 | Manufacturer | accessdata.fda.gov |
| Retractor | GAD | 1 | Manufacturer | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Manufacturer | accessdata.fda.gov |
| Speculum, Vaginal, Metal | HDF | 1 | Manufacturer | accessdata.fda.gov |
| Stethoscope Head | BZS | 1 | Manufacturer | accessdata.fda.gov |
| Stylet, Tracheal Tube | BSR | 1 | Manufacturer | accessdata.fda.gov |
| Syringe, Periodontic, Endodontic, Irrigating | EIC | 1 | Manufacturer | accessdata.fda.gov |
| Tube, Ear Suction | JZF | 1 | 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 |
|---|---|---|---|---|---|---|
| November 19, 2010 | K093495 | OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITS | HLJ | Substantially Equivalent | American Diagnostic Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Speculum, Vaginal, Metal
- All makers of Scissors, General, Surgical
- All makers of Laryngoscope, Rigid
- All makers of Forceps
- All makers of Retractor
- All makers of Tube, Ear Suction
Updated November 19, 2010. 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.