Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Acute Innovations with 5 510(k) clearances and 1 device recall. The most recent is a device recall dated Oct 30, 2013: The ACUTE Innovations Modular RibLoc System (RibLoc U plus) is comprised titanium plates….
| Oct 30, 2013 | The ACUTE Innovations Modular RibLoc System (RibLoc U plus) is comprised titanium plates and screws that are used to stabilize rib fracturesClass II · The ACUTE Innovations Ribloc U plus Rib Fracture Plating System is recalled because it has the potential to malfunction | Device recalls |
| Feb 17, 2012 | ACUTE INNOVATIONS BIOBRIDGE RESORBABLE PLATING SYSTEMK120163 · HRS | 510(k) clearances |
| Jan 12, 2012 | ACUTE INNOVATIONS MODULAR RIBLOC SYSTEMK113318 · HRS | 510(k) clearances |
| Sep 17, 2010 | ACUTE INNOVATIONS STERNAL FIXATION SYSTEMK101170 · KTT | 510(k) clearances |
| Sep 3, 2008 | RE-ZORB PLATING SYSTEMK081588 · HRS | 510(k) clearances |
| Jun 19, 2006 | ACUTE BONE SCREWK061206 · HWC | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
