Home › TheraMicro, LLC › TekBrace Solo

TekBrace Solo

TheraMicro, LLC · Model 2508S008 · UDI-DI 00810198920130

QUW FTL OWX Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Soft Tissue Reinforcement Device - 8cm

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 key Read 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.