Facility

SUN NUCLEAR CORPORATION

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1038814
Establishment type	Manufacture Medical Device
Location	3275 Suntree Blvd Melbourne, FL, US 32940
Registration status	Active · expires 2026
Parent company	SUN NUCLEAR CORPORATION (owner-operator 10028193)
Brand names	1049 - SunSILICON P; 1048 - SunSILICON; 1118 - EDGE DETECTOR

Activity by year

Recalls (1)

Devices registered here (1)

Accelerator, Linear, Medical
Product code IYE (opens in a new tab) · Class II · Radiology · 21 CFR 892.5050

Recalls & enforcement

Class IITerminated2014-08-08
Has a Potential Pinch Hazard to user performing Machine QA in an MRI environment.

All facilities operated by SUN NUCLEAR CORPORATION

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “SUN NUCLEAR CORPORATION (FEI 1038814) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1038814-sun-nuclear-corporation/

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