Data / Medical devices / United States / Typhoon Water Wares
Typhoon Water Wares: FDA-registered device maker in Pocomoke City, MD, United States, 1 510(k) clearance
Typhoon Water Wares is registered with the FDA (registration 1000402893) in Pocomoke City, MD, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 17, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1000402893
- Address
- 1106 Market St, Pocomoke City, MD, United States, 21851
- Owner or operator
- Typhoon Water Wares (10037097)
- Roles
- Manufacturer
- First device listed
- June 17, 2011
- Registered through
- 2026
- Brand names listed
- Class 4 Hyperbaric Chamber, Newtowne Hyperbarics
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chamber, Hyperbaric | CBF | 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 |
|---|---|---|---|---|---|---|
| November 17, 2005 | K051759 | FLEXI-LITE, MODEL FL-V1.2 | CBF | Substantially Equivalent | Performance Hyperbarics | accessdata.fda.gov |
Compare with other makers
Updated November 17, 2005. 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.