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Data / Medical devices / United States / Rehrig Pacific Company

Rehrig Pacific Company: FDA-registered device maker in Lawrenceville, GA, United States, 2 510(k) clearances

Rehrig Pacific Company is registered with the FDA (registration 3000186388) in Lawrenceville, GA, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated July 12, 2013. 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
3000186388
Address
1000 Raco Ct, Lawrenceville, GA, United States, 30046
Owner or operator
Rehrig Pacific Company (10038241)
Roles
Specification developer
First device listed
November 13, 2013
Registered through
2026
Brand names listed
Sharps Tank

Devices it lists

DeviceProduct codeClassRoleSource
Container, SharpsMMK2Specification developeraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
July 12, 2013K131087SHARPSTANK REUSABLE SHARPS CONTAINERMMKSubstantially EquivalentRehrig Pacific Companyaccessdata.fda.gov
April 25, 2012K111085SHARPS TANK REUSABLE SHARPS CONTAINERMMKSubstantially EquivalentRehrig Pacific Companyaccessdata.fda.gov

Compare with other makers

Updated July 12, 2013. 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.