Data / Medical devices / United States / Sharps Compliance, Inc.
Sharps Compliance, Inc.: FDA-registered device maker in Houston, TX, United States, 3 510(k) clearances
Sharps Compliance, Inc. is registered with the FDA (registration 3007508552) in Houston, TX, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated December 15, 2008. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3007508552
- Address
- 2730 Reed Rd. Suite 200, Houston, TX, United States, 77051
- Owner or operator
- SHARPS COMPLIANCE, INC. (9041198)
- Roles
- Specification developer
- First device listed
- April 27, 2000
- Registered through
- 2027
- Brand names listed
- 1-Gallon Sharps Collection Container, 1-Quart Sharps Collection Container, 1.5-Quart Sharps Collection Container, 2-Gallon Sharps Collection Container, 3-Gallon Sharps Collection Container, IV POLES, PITCH-IT, Transport Tube
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Sharps | MMK | 2 | Specification developer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Specification developer | accessdata.fda.gov |
| Stand, Infusion | FOX | 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 |
|---|---|---|---|---|---|---|
| December 15, 2008 | K083129 | SHARPS COMPLIANCE CONTAINER | MMK | Substantially Equivalent | Sharps Compliance, Inc. | accessdata.fda.gov |
| June 23, 2008 | K073577 | SHARPS TRANSPORT TUBE, MODEL 50035 | MMK | Substantially Equivalent | Sharps Compliance, Inc. | accessdata.fda.gov |
| December 14, 1994 | K945275 | PRO-TEC DISPOSBLE SHARPS CONTAINERS Q1 | FMI | Substantially Equivalent | Pro-Tec Containers, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Stand, Infusion
- All makers of Container, Sharps
Updated December 15, 2008. 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.