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 14, 2026, FDA's public records list J. T. Posey Company with 13 510(k) clearances and 1 device recall. The most recent is a device recall dated Oct 31, 2012: Posey Biothane Restraint Cuffs, Catalog Number 2900. The device is intended to limit ….
| Oct 31, 2012 | Posey Biothane Restraint Cuffs, Catalog Number 2900. The device is intended to limit a patient's movement to the extent necessary for treClass II · The firm voluntarily recalled Biothane Restraint Cuffs, Catalog No. 2900, that did not meet the required specifications | Device recalls |
| May 2, 2012 | POSEY BEDK113355 · OYS | 510(k) clearances |
| Mar 21, 2012 | POSEY BEDK113357 · OYS | 510(k) clearances |
| Apr 22, 2011 | POSEY BEDK103817 · OYS | 510(k) clearances |
| Nov 22, 1996 | JACKETS AND VESTSK963442 · FMQ | 510(k) clearances |
| Nov 22, 1996 | MULTIPLE BELTSK963414 · FMQ | 510(k) clearances |
| Nov 22, 1996 | POSEY STRAIGHT JACKETSK963410 · FMQ | 510(k) clearances |
| Nov 22, 1996 | RESTRAINT ACCESSORIESK963436 · FMQ | 510(k) clearances |
| Nov 19, 1996 | PEDIATRIC LIMB HOLDERSK963439 · FMQ | 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
