Data / Medical devices / United States / NeVap Inc Inventory Management
NeVap Inc Inventory Management: FDA-registered device maker in San Jose, CA, United States, 1 510(k) clearance
NeVap Inc Inventory Management is registered with the FDA (registration 3014544429) in San Jose, CA, United States. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 16, 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
- 3014544429
- Address
- 1265 Oakland Rd, San Jose, CA, United States, 95112
- Owner or operator
- NeVap Inc (10057984)
- Roles
- Specification developer
- First device listed
- June 21, 2018
- Registered through
- 2026
- Brand names listed
- Aspire Subglottic Suction Endotracheal Tube, SecureSwap ETT Holder System, Snapblock, Subglottic Introducer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheters, Suction, Tracheobronchial | BSY | 1 | Specification developer | accessdata.fda.gov |
| Device, Fixation, Tracheal Tube | CBH | 1 | Specification developer | accessdata.fda.gov |
| Endoscopic Bite Block | MNK | 1 | Specification developer | accessdata.fda.gov |
| Stylet, Tracheal Tube | BSR | 1 | Specification developer | accessdata.fda.gov |
| Tube, Tracheal (W/Wo Connector) | BTR | 2 | Specification developer | 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 16, 2018 | K172208 | NeVap Aspire Subglottic Suction Endotracheal Tube (ASSET) with Preloaded Stylet | BTR | Substantially Equivalent | Nevap, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Stylet, Tracheal Tube
- All makers of Tube, Tracheal (W/Wo Connector)
- All makers of Device, Fixation, Tracheal Tube
- All makers of Catheters, Suction, Tracheobronchial
- All makers of Endoscopic Bite Block
Updated February 16, 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.