FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 2 companies' records, each linked to the record.
As of Nov 14, 2026, FDA's public records list RTX and its 2 subsidiaries with 4 510(k) clearances and 2 device recalls. The most recent is a device recall dated Jan 29, 2019: TASE 400 Imaging systems.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, RTX and its 2 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 29, 2019 | TASE 400 Imaging systemsClass II · the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of im | Device recalls |
| Jan 29, 2019 | TASE 500 Imaging systemsClass II · the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of im | Device recalls |
| Apr 13, 1988 | BFGOODRICH BIOTHANE NON-ADHERENT DRESSINGK875253 · NAD | 510(k) clearances |
| Jun 30, 1987 | BIOFILM TRANS. POUCH ULCER & WOUND DRESSINGK872101 · NAD | 510(k) clearances |
| Jun 30, 1987 | BIOFILM TRANSORBENT ULCER AND WOUND DRESSINGK872100 · NAD | 510(k) clearances |
| Jun 30, 1987 | BIOFILM TRANS. ISLAND, ISLAND ULCER & WOUND DRESS.K872099 · NAD | 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
