Alto Development Corp.
5206 Asbury Road, FARMINGDALE, NJ, US
Registered product codes
13 product codes
Recent MDR events
29 on file
- MYO/WIREMar 25, 2026InjuryMW5185817
- ZIMMER BIOMET STERNALOCK XP RIGID FIXATION SYSTEMSep 22, 2025MalfunctionMW5176345
- STERNALOCK X RIGID FIXATION SYSTEM IMPLANT X CABLE PLATEMay 16, 2025MalfunctionMW5170518
- STERNALOCK XP RIGID FIXATION SYSTEMJun 17, 2024MalfunctionMW5156328
- DISPOSABLE SUCTION COAGULATORJul 25, 2023MalfunctionMW5120185
- STERNAL NEEDLE DOUBLE WIRE BALL.CS#3.USP#6.65MMApr 22, 2022MalfunctionMW5109307
- A&E MEDICAL 4.0 ROTATING SURGICAL PUNCHDec 22, 2020InjuryMW5098498
- WIRE TWSITERNov 15, 2016Malfunction6101842
- A&E MEDICAL MYOWIRE IIA&E MEDICAL MYOWIRE IIJul 22, 2015Malfunction4976121
- SUCTION COAGULATORJul 18, 2014Injury2242056-2014-00001
Recalls
7 on file
- TerminatedUnknown
Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes the through-channel for cable tensioning, rendering the tensioner inoperable.
View FDA record ↗ - TerminatedUnknown
Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes the through-channel for cable tensioning, rendering the tensioner inoperable.
View FDA record ↗ - TerminatedUnknown
Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes the through-channel for cable tensioning, rendering the tensioner inoperable.
View FDA record ↗ - TerminatedUnknown
Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes the through-channel for cable tensioning, rendering the tensioner inoperable.
View FDA record ↗ - TerminatedUnknown
Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes the through-channel for cable tensioning, rendering the tensioner inoperable.
View FDA record ↗ - TerminatedUnknown
Surgical punches are being recalled due to potential packaging damage which may have occurred during transportation resulting in loss of sterility.
View FDA record ↗ - TerminatedUnknown
Updated instructions for use: Ultra-Flex MYO/WIRE Monopolar pacing wire looped electrode (M-21 Series) to be consistent between electrode IFU and instructions for M-21 loop.
View FDA record ↗
Compliance history
Matched by FEI 2242056.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.