MOON SURGICAL, INC.

FDA Device Registration & Listing · San Carlos, CA, US · Registration 3026790309

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3026790309
FEI Number
3026790309
Entity Name
MOON SURGICAL, INC.
City/State/Country
San Carlos, CA, US
Establishment Address
619 Old County Road, San Carlos, CA 94070, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Moon Surgical SAS (Owner Number: 10087598)
Owner / Operator Contact Address
117 Quai de Valmy, Paris, FR-75 75010, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K242323
PMA Number
N/A

All Registered Proprietary Names

Maestro System Maestro System Maestro system

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQO Table, Operating-Room, Ac-Powered General, Plastic Surgery Class 1 878.4960 2024-08-30
QZB Software Controlled Endoscope And Instrument Holder Gastroenterology, Urology Class 2 876.1500 2025-07-07
QZB Software Controlled Endoscope And Instrument Holder Gastroenterology, Urology Class 2 876.1500 2025-03-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Moon Surgical SAS
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0036-2024 Getinge Usa Sales Inc 1
Meera Mobile Operating Table-to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment. Model Number: 7200.01F2

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026790309. Last updated year: 2026. Please use registration number 3026790309 when referencing this establishment in official correspondence.
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