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Sign in to claim this brandRESPONSIVE ORTHOPEDICS LLC
US
Last updated May 23, 2026
What RESPONSIVE ORTHOPEDICS LLC makes
RESPONSIVE ORTHOPEDICS LLC manufactures orthopedic devices including tibial inserts, knee tibia prosthesis trials, tendon/ligament bone anchors, instrument trays, uncoated knee femur prostheses, knee femur prosthesis trials, surgical drill guides, and fluted surgical drill bits.
The company's portfolio includes Class I and Class II devices listed in the FDA UDI registry and is based in the US.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What orthopedic devices does RESPONSIVE ORTHOPEDICS LLC manufacture?
RESPONSIVE ORTHOPEDICS LLC manufactures orthopedic devices including tibial inserts, knee tibia prosthesis trials, tendon/ligament bone anchors, instrument trays, uncoated knee femur prostheses, knee femur prosthesis trials, surgical drill guides, and fluted surgical drill bits.
Where is RESPONSIVE ORTHOPEDICS LLC based?
RESPONSIVE ORTHOPEDICS LLC is based in the United States, as indicated by the country designation in their device data.
Which regulatory registries list RESPONSIVE ORTHOPEDICS LLC's devices?
RESPONSIVE ORTHOPEDICS LLC's devices are listed in the FDA UDI registry, which tracks unique device identifiers for medical devices sold in the United States.
How are RESPONSIVE ORTHOPEDICS LLC's devices classified?
RESPONSIVE ORTHOPEDICS LLC manufactures both Class I and Class II medical devices. Class I devices are low-risk, while Class II devices require more regulatory controls but are still considered moderate-risk devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 080074787
Catalogue (744)
Page 9 of 15| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-192520 | FDA UDI | Class II | Active |
| Nighthawk | 906000-0003 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-192310 | FDA UDI | Class II | Active |
| Mustang Knotless | 285941 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-201201 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-130214 | FDA UDI | Class II | Active |
| Stealth All-Suture Anchor | 285949 | FDA UDI | Class II | Active |
| Superhawk | 908001-0300 | FDA UDI | Class I | Active |
| Eagle | 000617-0000-P01 | FDA UDI | Class I | Active |
| Spirit | 90-RAC-320900 | FDA UDI | Class I | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-180114 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-110110 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-160210 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-160516 | FDA UDI | Class II | Active |
| Spirit PEEK | 900001-0700 | FDA UDI | Class I | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-192314 | FDA UDI | Class II | Active |
| Spirit Titanium Screw | 901000-0830 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-410400 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-130212 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-170420 | FDA UDI | Class II | Active |
| Thunderbolt | 909004-0000 | FDA UDI | Class I | Active |
| Mini Stealth All-Suture Anchor | 911000-0002 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-160316 | FDA UDI | Class II | Active |
| Falcon | 907000-0920 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-141118 | FDA UDI | Class II | Active |
| Awl | 903006-0000-P01 | FDA UDI | Class I | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-351114 | FDA UDI | Class II | Active |
| Spirit PEEK | 900003-0000 | FDA UDI | Class I | Active |
| Thunderbolt | 285958 | FDA UDI | Class II | Active |
| Mustang Knotless Suture Anchor | 915000-4750 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-170410 | FDA UDI | Class II | Active |
| Lightning | 905002-0003 | FDA UDI | Class I | Active |
| Superhawk | 908007-0375-P01 | FDA UDI | Class I | Active |
| Lightning | 905004-0003 | FDA UDI | Class I | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-191618 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-160610 | FDA UDI | Class II | Active |
| Spirit PEEK Screw | 900000-0828 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-353126 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-110610 | FDA UDI | Class II | Active |
| Cobra | 902001-0000 | FDA UDI | Class II | Active |
| Thunderbolt | 909003-0000 | FDA UDI | Class I | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-800012 | FDA UDI | Class II | Active |
| Lightning Long | 905003-0003-P01 | FDA UDI | Class I | Active |
| Superhawk | 908007-0475-P01 | FDA UDI | Class I | Active |
| Hornet | 90-RAA-415200 | FDA UDI | Class I | Active |
| Lightning | 905000-0003 | FDA UDI | Class II | Active |
| Hornet | 90-RAA-410210 | FDA UDI | Class II | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-110316 | FDA UDI | Class II | Active |
| Thunderbolt | 909001-0000-P01 | FDA UDI | Class I | Active |
| Responsive Orthopedics Total Knee Arthroplasty System | 90-SRK-141316 | FDA UDI | Class II | Active |
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