Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

RESPONSIVE 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
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
080074787

Catalogue (744)

Page 13 of 15
DeviceModel / ReferenceRegistriesClassStatus
Spirit PEEK Screw 900000-0923
FDA UDI
Class IIActive
Nighthawk 906007-0003
FDA UDI
Class IActive
Thunderbolt 908003-0002-P06
FDA UDI
Class IActive
Falcon 907009-0700
FDA UDI
Class IActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-180610
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-120118
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-311500
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-130610
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-210103
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-142210
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-142614
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-200500
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-130320
FDA UDI
Class IIActive
Spirit Titanium Screw 901000-0820
FDA UDI
Class IIActive
Thunderbolt 285965
FDA UDI
Class IActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-353123
FDA UDI
Class IIActive
Spirit 90-RAC-310823
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-192516
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-300201
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-141220
FDA UDI
Class IIActive
Lightning 905007-0002
FDA UDI
Class IActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-180110
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-141520
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-141620
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-191412
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-300206
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-142216
FDA UDI
Class IIActive
Spirit PEEK Screw 900000-0935
FDA UDI
Class IIActive
Superhawk 908003-0001-P05
FDA UDI
Class IActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-191616
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-332500
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-170120
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-191512
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-170418
FDA UDI
Class IIActive
Spirit PEEK Screw 900000-1128
FDA UDI
Class IIActive
Lightning Long 905002-0003-P01
FDA UDI
Class IActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-160220
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-180618
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-142218
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-800014
FDA UDI
Class IIActive
Hornet 903002-4500
FDA UDI
Class IActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-142620
FDA UDI
Class IIActive
Lightning 90-RAA-857110
FDA UDI
Class IActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-141212
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-130210
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-160616
FDA UDI
Class IIActive
Spirit Titanium Screw 901000-1020
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-191218
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-400021
FDA UDI
Class IIActive
Responsive Orthopedics Total Knee Arthroplasty System 90-SRK-160318
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.