Data / Medical devices / United States / Ims, Inc.
Ims, Inc.: FDA-registered device maker in Bixby, OK, United States, 1 510(k) clearance
Ims, Inc. is registered with the FDA (registration 3007421906) in Bixby, OK, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 26, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007421906
- FEI number
- 3003459352
- Address
- 12311 S 74th E Ave Suite A, Bixby, OK, United States, 74008
- Owner or operator
- IMS, Inc. (10043734)
- Roles
- Specification developer
- First device listed
- March 15, 2013
- Registered through
- 2026
- Brand names listed
- SureCare Gloves
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Latex Patient Examination Glove | LYY | 1 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| June 26, 2003 | K031414 | POWDER-FREE LATEX PATIENT EXAMINATION GLOVE, WHITE (NON-COLORED), OR BLUE COLORED, WITH EXTRACTABLE PROTEIN CONTENT LABE | LYY | Substantially Equivalent | Perusahaan Getah Asas Sdn. Bhd. | accessdata.fda.gov |
Compare with other makers
Updated June 26, 2003. 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.