Facility

STINGRAY SURGICAL PRODUCTS

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

Key facts

1recalls · worst Class II

4inspections · worst VAI

—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)	3006059917
Establishment type	Repack or Relabel Medical Device
Location	1701 Costa Del Sol Boca Raton, FL, US 33432
Registration status	Active · expires 2026
Parent company	Stingray Surgical Products (owner-operator 10026274)

Activity by year

Recalls (1)
Inspections (4)

Devices registered here (1)

Electrosurgical, Cutting & Coagulation & Accessories
Product code GEI (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4400

Recalls & enforcement

Class IITerminated2012-05-23
On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a recall initiated due to "Instructions For Use" of Bipolar Forceps not being cleared by FDA and incorrect "Instructions For Use" . The sterilization instructions have been altered without the clearance of…

FDA inspections (4)

NAI2024-12-11
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2023-02-09
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2019-12-20
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
VAI2016-11-22
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by Stingray Surgical Products

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. “STINGRAY SURGICAL PRODUCTS (FEI 3006059917) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006059917-stingray-surgical-products/

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