Data / Medical devices / Allergen And Vaccine Delivery Needles / United States
FDA-registered makers of Allergen And Vaccine Delivery Needles in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Allergen And Vaccine Delivery Needles (product code SCL). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Allergen And Vaccine Delivery Needles
- Product code
- SCL
- Country
- United States
Makers of Allergen And Vaccine Delivery Needles in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Lincoln Diagnostics, Inc. | Decatur, IL, United States | Manufacturer | 3 | August 7, 1996 | 0 | 0 | 0 | api.fda.gov |
| Roechling Medical Lancaster, LLC | Denver, PA, United States | Manufacturer | 2 | August 7, 2003 | 0 | 0 | 0 | api.fda.gov |
| Alkaline Corp. | Eatontown, NJ, United States | Manufacturer | 1 | February 8, 1985 | 0 | 0 | 0 | api.fda.gov |
| Allergy & Applicator Depot, LLC | Manorville, NY, United States | Specification developer | 1 | April 10, 2019 | 0 | 0 | 0 | api.fda.gov |
| Greer Laboratories, Inc. | Lenoir, NC, United States | Manufacturer, Specification developer | 1 | June 23, 1989 | 0 | 0 | 0 | api.fda.gov |
| Jubilant Hollisterstier LLC | Spokane, WA, United States | Manufacturer, Specification developer | 1 | November 13, 1995 | 0 | 0 | 0 | api.fda.gov |
| Medscience Research Group, Inc. | West Palm Beach, FL, United States | Specification developer | 1 | March 5, 2018 | 0 | 0 | 0 | api.fda.gov |
| BioGeniv, INC | Lenoir, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.