FDA Device Intelligence
Home › The Flex Company › Flex Cup

Flex Cup

The Flex Company · Model Single Flex Cup Full Fit (Size 2) box · UDI-DI 00851906007200

HHE
10
510(k) clearances
553
Adverse events
0
Recalls
77
Facilities

Description

Single Flex Cup Full Fit (Size 2), English only

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.