Data / Medical devices / Saudi Arabia / United Medical Industries Co. Ltd.
United Medical Industries Co. Ltd.: FDA-registered device maker in RIYADH Ar Riyad, Saudi Arabia, 10 510(k) clearances
United Medical Industries Co. Ltd. is registered with the FDA (registration 3004117249) in RIYADH Ar Riyad, Saudi Arabia. It lists 7 device types. The FDA files 10 510(k) clearances under its listings, the newest dated November 7, 2007. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3004117249
- Address
- Street # 215, 3rd Industrial City, P.O. Box 51871 Riyadh -11553, RIYADH Ar Riyad, Saudi Arabia, 11553
- Owner or operator
- UNITED MEDICAL INDUSTRIES CO. LTD. (9057826)
- Roles
- Manufacturer
- First device listed
- November 22, 2007
- Registered through
- 2026
- Brand names listed
- UNICAPRONE, UNICRYL, UNICRYL M, UNICRYL quick, UNIESTER / UNIESTER C, UNIGLACTIN, UNIMIDE / UNIMIDE B / UNIMIDE C, UNIPLAIN / UNICHROME and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Suture, Absorbable, Natural | GAL | 2 | Manufacturer | accessdata.fda.gov |
| Suture, Absorbable, Synthetic, Polyglycolic Acid | GAM | 2 | Manufacturer | accessdata.fda.gov |
| Suture, Nonabsorbable, Silk | GAP | 2 | Manufacturer | accessdata.fda.gov |
| Suture, Nonabsorbable, Synthetic, Polyamide | GAR | 2 | Manufacturer | accessdata.fda.gov |
| Suture, Nonabsorbable, Synthetic, Polyethylene | GAT | 2 | Manufacturer | accessdata.fda.gov |
| Suture, Nonabsorbable, Synthetic, Polypropylene | GAW | 2 | Manufacturer | accessdata.fda.gov |
| Suture, Surgical, Absorbable, Polydioxanone | NEW | 2 | 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 7, 2007 | K072646 | UNICAPRONE | GAM | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
| November 7, 2007 | K072645 | UNIGLACTIN | GAM | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
| November 7, 2007 | K072644 | UNICRYL QUICK | GAM | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
| September 7, 2005 | K042287 | UNIPLAIN & UNICHROM | GAL | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
| December 27, 2004 | K042288 | UNICRYL | GAM | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
| December 10, 2004 | K042285 | UNICRYL M | NEW | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
| December 3, 2004 | K042284 | UNIMIDE | GAR | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
| December 1, 2004 | K042286 | UNIESTER C | GAT | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
| December 1, 2004 | K042283 | UNIPRO | GAW | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
| December 1, 2004 | K042282 | UNISILK | GAP | Substantially Equivalent | United Medical Industries Co. , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Suture, Absorbable, Synthetic, Polyglycolic Acid
- All makers of Suture, Surgical, Absorbable, Polydioxanone
- All makers of Suture, Absorbable, Natural
- All makers of Suture, Nonabsorbable, Synthetic, Polyamide
- All makers of Suture, Nonabsorbable, Silk
- All makers of Suture, Nonabsorbable, Synthetic, Polyethylene
Updated November 7, 2007. 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.