FirmLabelled 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 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list AlloSource with 4 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Jun 27, 2023: AceConnex Pre-Sutured Fascia.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jun 27, 2023 | AceConnex Pre-Sutured FasciaK213046 · GAT | 510(k) clearances |
| Mar 20, 2018 | ReConnex Pre-Sutured TendonK170957 · GAT | 510(k) clearances |
| Mar 25, 2014 | AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic applications as filler for gaps or voids that are not iClass II · The donor was hemodiluted. | Device recalls |
| Jan 10, 2011 | ALLOFUSE PLUSK103036 · MQV | 510(k) clearances |
| Dec 4, 2008 | ALLOFUSE GEL AND PUTTYK071849 · MQV | 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
