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Sign in to claim this brandAPPLIED MEDICAL RESOURCES CORP.
United States·US-MF-000000764
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 22872, Avenida Empresa, Rancho Santa Margarita, CA, United States
- Website
- appliedmedical.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Leilani Domingo
- EUDAMED SRN
- US-MF-000000764
- FDA FEI Number
- 2027111
- DUNS Number
- —
Catalogue (1347)
Page 25 of 27| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Master Surgeon's Lap Chole Kit | K2654 | FDA UDI | Class II | Active |
| Dr. Poynter Amrc | K2590 | FDA UDI | Class II | Active |
| 5MM Fios® SURGICAL KIT | K0902 | FDA UDI | Class II | Active |
| TOTAL 5mm SOLUTION KIT 8 | GK150 | FDA UDI | Class II | Active |
| 5mm CLIP/NON-BLADED TROCARS | K2803 | FDA UDI | Class II | Active |
| Syntel Thrombectomy Catheter | A4538 | FDA UDI | Class II | Active |
| Lap Chole Kit - 1a | K0522 | FDA UDI | Class II | Active |
| Cus Universal Kit | K2527 | FDA UDI | Class II | Active |
| Ke050 Lap | GK237 | FDA UDI | Class II | Active |
| Ej943p | EJ943P | FDA UDI | Class II | Unknown |
| Kii Shielded Bladed Access System | CFB01 | FDA UDI | Class II | Active |
| Soft/Traction Clamp Inserts | A0802 | FDA UDI | Class II | Active |
| Soft / Soft | G-8605 | FDA UDI | Class II | Active |
| TOTAL 5mm SOLUTION KIT 11 | GK153 | FDA UDI | Class II | Active |
| Applied Standard Ureteral Stent with SL-6® Hydrophilic Coating and Tether | B3653 | FDA UDI | Class II | Unknown |
| Whitworth Lc | K2667 | FDA UDI | Class II | Active |
| Lap Chole Kit | K2452 | FDA UDI | Class II | Active |
| Dr. Melarvie's Lap Chole Pack | K2681 | FDA UDI | Class I | Active |
| TOTAL 5mm SOLUTION KIT 10 | GK152 | FDA UDI | Class II | Active |
| Lap Chole /osu East | K2848 | FDA UDI | Class II | Active |
| MIGS Kit 1 | GK158 | FDA UDI | Class II | Active |
| Lap Chole Kit-Ahmc Monterey Park | K2371 | FDA UDI | Class II | Active |
| Kii® Separator Access System | C0Q87 | FDA UDI | Class II | Unknown |
| Syntel Thrombectomy Catheter | A4548 | FDA UDI | Class II | Active |
| Silhouette® Xtraflo Ureteral Stent | B3851 | FDA UDI | Class II | Active |
| Standard Set 374 F | GK249 | FDA UDI | Class II | Active |
| Dr. Alexander's Lap Chole Kit | K2282 | FDA UDI | Class II | Active |
| Sterile Specimen Collection Swab | NPS19 | FDA UDI | Class I | Active |
| Convertible Trocar System | C0F04 | FDA UDI | Class II | Active |
| Kii Low Profile Bladed Access System | CTB21 | FDA UDI | Class II | Active |
| Scope Warmer Base | C3002 | FDA UDI | Class II | Active |
| BARD Latex-free Arterial Embolectomy Catheters | CE0780 | FDA UDI | Class II | Active |
| Kii® Optical Access System | C0Q19 | FDA UDI | Class II | Active |
| Surgical Trocar And Cannula | K932995 | FDA 510(k) | Class II | Active |
| Cholangiography Clamp | K924480 | FDA 510(k) | Class I | Active |
| Epix Electrosurgical Probe with Smoke Evacuation | K151480 | FDA 510(k) | Class II | Active |
| Urological Guidwire | K944135 | FDA 510(k) | Class II | Active |
| Tissue Containment System; 10, 14, 17, 25 | K142427 | FDA 510(k) | Class II | Active |
| Latis Graft Cleaning Catheter | K973465 | FDA 510(k) | Class II | Active |
| Applied Ureteral Catheter | K020577 | FDA 510(k) | Class II | Active |
| Applied Access Seal | K012968 | FDA 510(k) | Class II | Active |
| Ureteral Access Sheath Set - New Models | K993650 | FDA 510(k) | Class II | Active |
| Endoscope Accessory | K931895 | FDA 510(k) | Class II | Active |
| Alexis Wound Retractor | K031889 | FDA 510(k) | Class II | Active |
| Wound Protector/Retractor | K020435 | FDA 510(k) | Class II | Active |
| GelPOINT Transvaginal Access Platform | K143308 | FDA 510(k) | Class II | Active |
| Voyant Maryland Fusion Device | K200598 | FDA 510(k) | Class II | Active |
| Applied Laparoscopic Disposable Monopolar Scissors | K062169 | FDA 510(k) | Class II | Active |
| Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302) | K253531 | FDA 510(k) | Class II | Active |
| Voyant Open Fusion Device | K162676 | FDA 510(k) | Class II | Active |
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