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Rocket Medical Plc

US

Last updated May 27, 2026

What Rocket Medical Plc makes

The company manufactures single-use and reusable medical devices for gynecological procedures, including intrauterine curettes and suction systems for uterine tissue removal, as well as catheter sets for assisted reproduction and pneumothorax drainage. It also produces IVF-specific tools such as oocyte aspiration needles and needle guides, alongside reusable cervical dilators and intrauterine imaging catheters. Electrocautery system electrodes for surgical precision are part of its portfolio, catering to both reproductive and thoracic applications.

The portfolio includes devices classified under FDA regulations as Class I and Class II, with authorisations granted through 510(k) clearances and Unique Device Identifiers (UDIs). These products are listed in the FDA’s regulatory databases, ensuring compliance with U.S. medical device standards. The company operates from the United States, adhering to domestic regulatory requirements for these categories.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Rocket Medical Plc manufacture?

Rocket Medical Plc specializes in medical devices primarily used in gynecological and reproductive procedures. Their portfolio includes single-use and reusable devices such as intrauterine curettes and suction systems for uterine tissue removal, catheter sets for assisted reproduction and pneumothorax drainage, IVF-specific tools like oocyte aspiration needles and needle guides, reusable cervical dilators, intrauterine imaging catheters, and electrocautery system electrodes. These devices cater to both reproductive health and thoracic applications.

Where is Rocket Medical Plc based, and how does this affect its regulatory compliance?

Rocket Medical Plc is based in the United States, which means its devices must comply with U.S. regulatory requirements. Since the company’s products fall under FDA classifications—such as Class I and Class II—they undergo evaluation through processes like 510(k) clearances and Unique Device Identifier (UDI) registration to ensure adherence to U.S. medical device standards.

Which regulatory databases list Rocket Medical Plc’s devices?

Rocket Medical Plc’s devices are listed in the FDA’s regulatory databases, specifically through the 510(k) clearance process and Unique Device Identifier (UDI) registration. These listings confirm that the devices meet U.S. regulatory requirements for their respective classifications, ensuring traceability and compliance.

How are Rocket Medical Plc’s devices classified under FDA regulations?

Rocket Medical Plc’s devices are classified under FDA regulations as either Class I or Class II. Class I devices generally pose the lowest risk and may require less stringent regulatory oversight, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway, such as 510(k) clearance or other authorisation processes.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+4401914196988
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
544313588

Catalogue (236)

Page 3 of 5
DeviceModel / ReferenceRegistriesClassStatus
Rocket R57525-00-EV
FDA UDI
N/AActive
Rocket R58800-08-SD
FDA UDI
N/AActive
Rocket R28406
FDA UDI
Class IIUnknown
Rocket R54549-32-PK
FDA UDI
Class IActive
Rocket R51549-24-PK
FDA UDI
N/AActive
Rocket R57803
FDA UDI
N/AActive
Rocket R57851
FDA UDI
N/AActive
Rocket R28135
FDA UDI
Class IIUnknown
Rocket R57973
FDA UDI
N/AActive
Rocket R51549-26-PK
FDA UDI
N/AActive
Rocket R57980
FDA UDI
N/AActive
Rocket R57032
FDA UDI
N/AActive
Rocket R50000
FDA UDI
N/AActive
Rocket R58800-84-30
FDA UDI
N/AActive
Rocket R57631-EC-23
FDA UDI
N/AActive
Rocket R57040
FDA UDI
N/AActive
Rocket R57424-VIP
FDA UDI
Class IIUnknown
Rocket R57509
FDA UDI
N/AActive
Rocket R57998
FDA UDI
N/AActive
Rocket R57958
FDA UDI
N/AActive
Rocket R54410-WB-DL
FDA UDI
Class IIActive
Rocket R51400-16-00
FDA UDI
N/AActive
Rocket R57512
FDA UDI
N/AActive
Rocket R57525-00-ED
FDA UDI
N/AActive
Rocket R57631-00-23
FDA UDI
N/AActive
Rocket R57603-00-90
FDA UDI
N/AUnknown
Rocket R54549-28-PK
FDA UDI
N/AActive
Rocket R57710-SX-70
FDA UDI
N/AActive
Rocket R57034
FDA UDI
N/AActive
Rocket R57635-00-23
FDA UDI
N/AActive
Rocket R57035
FDA UDI
N/AActive
Rocket R51549-18-PK
FDA UDI
N/AActive
Rocket R54509
FDA UDI
Class IActive
Rocket R57525-00-E2
FDA UDI
N/AActive
Rocket R51400-MI-PL
FDA UDI
N/AActive
Rocket R29661
FDA UDI
Class IIActive
Rocket R57036
FDA UDI
N/AActive
Rocket R54960-DG-FX
FDA UDI
N/AActive
Rocket R57602-SX-90
FDA UDI
N/AActive
Rocket R57635-EC-23
FDA UDI
N/AActive
Rocket R57420
FDA UDI
N/AActive
Rocket R51400-DP
FDA UDI
N/AActive
Rocket R57591
FDA UDI
N/AActive
Rocket R57679
FDA UDI
N/AActive
Rocket R51401-16-PT
FDA UDI
N/AActive
Rocket R57972
FDA UDI
N/AActive
Rocket R58800-08-NK
FDA UDI
N/AActive
Rocket R57525-00-AK
FDA UDI
N/AActive
Rocket R57422-VIP
FDA UDI
Class IIUnknown
Rocket R57591-BT-18
FDA UDI
N/AActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Rocket Medical Plc WASHINGTON Sunderland · GB FEI 3002808026