Data / Medical devices / United States / Alkaline Corp.
Alkaline Corp.: FDA-registered device maker in Eatontown, NJ, United States, 1 510(k) clearance
Alkaline Corp. is registered with the FDA (registration 2248704) in Eatontown, NJ, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 8, 1985. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 2248704
- FEI number
- 1000526882
- Address
- 38 Industrial Way E Ste 3A, Eatontown, NJ, United States, 07724
- Owner or operator
- ALKALINE CORP. (9023828)
- Roles
- Manufacturer
- First device listed
- October 17, 2008
- Registered through
- 2026
- Brand names listed
- Morrow Brown Allergy Test Needle
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Allergen And Vaccine Delivery Needles | SCL | 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 |
|---|---|---|---|---|---|---|
| February 8, 1985 | K844221 | HMB ALLERGOGEN SKIN PRICK TEST NEEDLE | SCL | Substantially Equivalent | Aller/Guard, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 8, 1985. 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.