Data / Medical devices / United States / Perrigo New York, Inc.
Perrigo New York, Inc.: FDA-registered device maker in Bronx, NY, United States, 1 510(k) clearance
Perrigo New York, Inc. is registered with the FDA (registration 2434221) in Bronx, NY, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 9, 2018. 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
- 2434221
- FEI number
- 2450054
- Address
- 1700 Bathgate Ave, Bronx, NY, United States, 10457
- Owner or operator
- PERRIGO COMPANY (9924144)
- Roles
- Manufacturer
- First device listed
- October 10, 2018
- Registered through
- 2026
- Brand names listed
- Personal Lubricating Jelly
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 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 |
|---|---|---|---|---|---|---|
| July 9, 2018 | K180923 | Personal Lubricating Jelly | NUC | Substantially Equivalent | Perrigo New York, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 9, 2018. 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.