Buying guide
Ottava
By Johnson & Johnson · surgical
- Price
- —
- Availability
- Internal use only (not for retail).
- Maturity
- pilot
- Real-world use
- Yes, 1 verified deployment
J&J MedTech's Ottava is a soft-tissue general-surgery robotic platform with four arms integrated into the operating table, announced in 2020. It is pre-market: J&J submitted a De Novo request to the FDA in January 2026, and Ottava is not authorized to be marketed. DEPLOY classifies it research tier: J&J's corporate scale does not translate into verified surgical-robotics deployment, because the gating event (FDA clearance) has not occurred. By the framework, Ottava sits at the same research tier as far smaller pre-market entrants. There is no price; it is not sold.
Readiness
Ottava is internal use only (not for retail), no capability claims are on file, 1 verified deployment is on file, and no incidents are on record.
- Availability
- internal-only
Internal use only (not for retail).
- Price honesty
- no-price
No price points on file for Ottava.
- Capability honesty
- no-claims
No reviewed capability claims on file for Ottava.
- Real-world use
- pilot
Maturity: pilot. 1 verified deployment in the registry.
- Safety record
- no-incidents
No incidents on record. 1 verified deployment on file.
What it claims to do
No reviewed capability claims on file.
Price
No reviewed price points on file.
Real-world use
- United States2024-01-01
Safety record
No incidents on record. 1 verified deployment on file.
Privacy
No privacy practices disclosed or on file for Ottava.
Specs
- arms
- four
- notes
- Verified (pre-market): Johnson & Johnson (NYSE: JNJ; founded 1886, New Brunswick NJ; MedTech/Ethicon division) submitted Ottava to the FDA via a De Novo classification application on Jan 7 2026 for multiple upper-abdomen general-surgery procedures. J&J's own language: Ottava 'is under development and is not authorized to be marketed or sold in any market.' IDE first cases completed early 2025 at Memorial Hermann-Texas Medical Center; a second IDE (inguinal hernia) approved late 2025.
- Maturity = research (FDA gating not cleared): Per the framework, NO clearance = research-tier regardless of corporate scale or demos. Ottava has an active IDE and a pending De Novo submission but no clearance and ZERO installed base / zero approved procedures (IDE-trial cases only).
- Aggregator-drift correction: A secondary source claimed Ottava was 'targeted for commercial launch late 2025 / early 2026.' CONTRADICTED by the primary J&J source (De Novo submitted Jan 7 2026; explicitly not marketable). Do NOT register a launch date. 'Breakthrough device designation' (secondary) is unverified against primary records.
- Adjacent J&J robotics (context, not this entity): Monarch (robotic bronchoscopy, via the 2019 $3.4B Auris acquisition; FDA-cleared; competes with Intuitive Ion) and Velys (robotic knee replacement, FDA-cleared Mar 2021) are separate commercial J&J robotics products.
- products
- Ottava: J&J MedTech (Ethicon) soft-tissue general-surgery robotic platform, four arms integrated into the operating table; announced 2020. NOT cleared, NOT marketed.
- formFactor
- surgical (unified-architecture four-arm soft-tissue general-surgery robot; arms integrated into the table)
- fda_clearance
- not cleared
- procedure_types
- multiple upper-abdomen general-surgery procedures
What's under the hood
No brain on file for Ottava.
Frequently asked questions
- Is the Ottava actually available for purchase?
- Not available to consumers. In internal use by Johnson & Johnson.Source: J&J submits Ottava to FDA (De Novo, Jan 7 2026; 'not authorized to be marketed')
- What does the Ottava cost?
- Not announced.
- Where is the Ottava being used?
- Ottava is in use at: United States (2024-01-01).Source: J&J MedTech Ottava product page
- Is the Ottava safe?
- No incidents on record across 1 verified deployment.
- How does the Ottava handle privacy?
- No privacy practices disclosed or on file for Ottava.
- Who makes the Ottava?
- Ottava is made by Johnson & Johnson, based in New Brunswick, New Jersey, USA.Source: J&J submits Ottava to FDA (De Novo, Jan 7 2026; 'not authorized to be marketed')
Video
Johnson & Johnson MedTech's surgical-robotics brand film, which features its Ottava soft-tissue surgical robot (no Ottava-specific video exists on the official channel). A surgeon-teleoperated system, not autonomous.
Manufacturer
Johnson & Johnson (registry record: /companies/johnson-and-johnson)
Compare side by side
- Ottava vs Hugo RASby Medtronic · surgical
Sources
- J&J submits Ottava to FDA (De Novo, Jan 7 2026; 'not authorized to be marketed') · https://www.jnj.com/media-center/press-releases/johnson-johnson-submits-ottava-robotic-surgical-system-to-the-u-s-food-and-drug-administration
- J&J robotics layoffs + Ottava delays (history/context) · https://www.medtechdive.com/news/jnj-layoffs-auris-california-robotic/644544/
- J&J takes over Verb Surgical (Ottava lineage) · https://www.fiercebiotech.com/medtech/jj-to-take-over-verb-surgical-its-robotics-venture-verily
- J&J MedTech Ottava product page · https://www.jnjmedtech.com/en-US/product/ottava
- J&J Ottava press releases · https://www.jnj.com/tag/ottava
Recent coverage
- DePuy Synthes Appoints Andrew Burton as Global Head of Robotics - hrtoday.inGoogle News · 2026-06-27
- J&J submits FDA de novo request for Ottava robot in general surgeryAgentRecon · 2026-06-17
- J&J’s DePuy Synthes has a new head of robotics platforms - MassDeviceGoogle News · 2026-06-12
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