Medical device makerLabelled 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 13, 2026, FDA's public records list Alto Development Corp. with 10 510(k) clearances and 7 device recalls. The most recent is a device recall dated Sep 10, 2019: A&E Medical Thorecon Plating System Kits Model No. 94-1400-04. For fracture fixation or….
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 |
|---|---|---|
| Sep 10, 2019 | A&E Medical Thorecon Plating System Kits Model No. 94-1400-04. For fracture fixation or reconstruction of the sternum.Class II · Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes th | Device recalls |
| Sep 10, 2019 | A&E Medical Thorecon Plating System Kits Model No. 94-1700-10. For fracture fixation or reconstruction of the sternum.Class II · Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes th | Device recalls |
| Sep 10, 2019 | A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For fracture fixation or reconstruction of the sternum.Class II · Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes th | Device recalls |
| Sep 10, 2019 | A&E Medical Thorecon Plating System Kits Model No. 94-1500-04-S. For fracture fixation or reconstruction of the sternum.Class II · Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes th | Device recalls |
| Sep 10, 2019 | A&E Medical Thorecon Plating System Kits Model No. 94-1300-04-S. For fracture fixation or reconstruction of the sternum.Class II · Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes th | Device recalls |
| Jun 21, 2019 | A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire Looped Electrode (M-21 SERIES)- Temporary Pacing Electrode as followClass II · Updated instructions for use: Ultra-Flex MYO/WIRE Monopolar pacing wire looped electrode (M-21 Series) to be consistent | Device recalls |
| Oct 23, 2017 | Surgical punch; sealed pouches packed in punch shelf box Intended for use by trained surgeons to create circular cuts in soft tissue or Class II · Surgical punches are being recalled due to potential packaging damage which may have occurred during transportation resu | Device recalls |
| Dec 20, 1996 | A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTONK964621 · GEI | 510(k) clearances |
| Jan 7, 1994 | LABELING FOR MYO/WIRE II STERNOTOMY SUTURESK932513 · GAO | 510(k) clearances |
| Sep 7, 1993 | A&E MEDICAL ELECTROSURG ELECTRO W/NON-STICK COATK931537 · GEI | 510(k) clearances |
| May 17, 1993 | A&E MEDICAL ELECTROSURGICAL CONNECTING CORDSK930528 · GEI | 510(k) clearances |
| Oct 5, 1992 | A&E MEDICAL CORP DISPOS SUCT COAG W/NON STICK COATK914193 · GEI | 510(k) clearances |
| Feb 18, 1992 | A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIESK915300 · GEI | 510(k) clearances |
| Nov 30, 1988 | RANEY CLIPK884783 · FZQ | 510(k) clearances |
| Apr 21, 1988 | ELECTRO-CAUTERY SUCTION TUBEK881413 · GEI | 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
