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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 94 of 96| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Stingray Surgical Products | S03-682TRD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-676RSD20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-167NSD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-418NSR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-128NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-696RSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S031-631NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-102NSSS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-653TU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-455NSR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-600NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-163NS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-695RS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-680R | FDA UDI | Class II | Active |
| Stingray Surgical Products | G03-014 | FDA UDI | Class I | Active |
| Stingray Surgical Products | S03-677NSSU30 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-455NSD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-683TRU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-682TD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-674SD20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-680TRD30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-675TSD20 | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-358S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-697TU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-568NSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-641TR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-530NSU20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-684NSR | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-467SPU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-681U30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-695S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-699TRSD20 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-653NSS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-064TS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-362 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-543NSRU45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-396S | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-096NSSS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-332 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-682R | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-547SPD45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-699TRU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-055TS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-683NSSU30 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S03-651NSR | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-098S | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-695TS | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-678TR | FDA UDI | Class II | Unknown |
| Stingray Surgical Products | S03-653U45 | FDA UDI | Class II | Active |
| Stingray Surgical Products | S02-648RSU30 | FDA UDI | Class II | Active |
Related Companies
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Authorities
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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. |