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Sign in to claim this brandSTINGRAY SURGICAL PRODUCTS
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 1701 Costa Del Sol, Boca Raton, FL, 33432
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3006059917
- DUNS Number
- —
Catalogue (4782)
Page 96 of 96| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Stingray Surgical Products | S02-655U20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-230FGD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-681NSR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-138NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-412NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-699SD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-698TRD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-698SD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-583NSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-685TSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-677TRS | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S02-651TRD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-545NSRU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-652TRSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-676RSU20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-230FGU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-695NSRSU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-655RS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-394NSRD45 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-655RSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-675D20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-469NSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-446 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-577NSU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-675SU20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-681D20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-682SU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-685D30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-392SPD30 | FDA UDI | Class II | Active |
| Stingray Ultralite Disposable Irrigating Bipolar Forceps | K102752 | FDA 510(k) | Class II | Active |
| Stingray Electrosurgical Forceps | K083162 | FDA 510(k) | Class II | Active |
| Stingray Bipolar Forceps | K123478 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 23, 2012 | Z-2011-2012 | — | terminated | 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 the FDA. |