Data / Medical devices / United States / Avery Biomedical Devices, Inc.
Avery Biomedical Devices, Inc.: FDA-registered device maker in Commack, NY, United States, 1 PMA approval
Avery Biomedical Devices, Inc. is registered with the FDA (registration 2427696) in Commack, NY, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated January 5, 1987. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 2427696
- Address
- 61 Mall DR, Commack, NY, United States, 11725
- Owner or operator
- AVERY BIOMEDICAL DEVICES, INC. (2427696)
- Roles
- Manufacturer
- First device listed
- November 1, 2007
- Registered through
- 2027
- Brand names listed
- Breathing Pacemaker
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Implanted Diaphragmatic/Phrenic Nerve Stimulator | GZE | 3 | Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| January 5, 1987 | P860026 | DIAPHRAGMATIC PACEMAKER PHRENIC NERVE STIMULATOR | GZE | 9 | November 4, 2019 | accessdata.fda.gov |
Updated November 4, 2019. 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.