Johnson & Johnson MedTech Ottava

Limited deployment Medical · #6
Index score 72.3 (#39 overall) · FDA De Novo marketing authorization granted July 22, 2026 for ten general surgery procedures; commercial rollout just beginning, so availability remains limited. · Last verified 2026-09-01

Ottava is Johnson & Johnson MedTech's soft-tissue surgical robot and the newest FDA-authorized entrant, granted De Novo marketing authorization on July 22, 2026 for ten general surgery procedures. Its defining feature is architecture: four nine-jointed arms are built directly into the operating table and stow beneath it, which J&J says cuts OR footprint by 30-50% versus boom-and-cart systems. Commercial rollout is just beginning, so availability is limited.

  • FDA De Novo authorization on July 22, 2026 covers ten general surgery procedures, ending da Vinci's long US soft-tissue robotic near-monopoly alongside Hugo [source]
  • In the pivotal 30-patient bariatric study, Ottava met its primary safety and performance endpoints with all procedures completed robotically, no conversions [source]
  • A US IDE clinical trial of Ottava in inguinal hernia procedures is underway [source]

Specifications

SpecificationValueConfidenceSource
Arms 4 robotic arms integrated directly into the operating table verified jnjmedtech.com (2026-09-01)
Architecture First table-integrated soft-tissue robotic system; arms stow beneath the table when not in use verified jnjmedtech.com (2026-09-01)
Arm articulation 9 joints per arm for anatomical access and collision avoidance reported medtechdive.com (2026-09-01)
OR footprint 30-50% less space than boom-and-cart systems, per J&J reported medtechdive.com (2026-09-01)
Setup automation Push-button movement into predefined procedural arm poses verified jnjmedtech.com (2026-09-01)
US indications 10 general surgery procedures including gastric bypass, gastric sleeve, cholecystectomy, appendectomy and hiatal hernia repair verified jnj.com (2026-09-01)

Every spec is cited to its source with a retrieval date. verified = manufacturer-published · reported = reputable press/analyst. Verify with the manufacturer before purchase decisions.

Change timeline

  1. milestone
    FDA grants De Novo marketing authorization for ten general surgery procedures [source]
  2. milestone
    J&J submits Ottava to FDA for De Novo classification [source]

Our take

Ottava's table-integrated design is the most genuinely different architecture to reach the US market, and J&J can pair it with its Ethicon instruments business. But it launches years behind da Vinci's ecosystem and slightly behind Hugo's US entry, with an initial indication set focused on upper-abdomen general surgery. Hospital buyers should treat 2026-2027 as Ottava's proving period: watch real-world uptime, instrument breadth and how fast indications expand.

Best suited for

  • Bariatric surgery (gastric bypass, gastric sleeve)
  • Cholecystectomy and hiatal hernia repair
  • Other upper-abdomen general surgery procedures within the authorized set

Ottava: common questions

Is the J&J Ottava robot FDA approved?
Yes. The FDA granted De Novo marketing authorization on July 22, 2026 for ten general surgery procedures, following J&J's submission in January 2026.
Can hospitals buy Ottava now?
Rollout is only beginning as of late 2026 and J&J has described a staged launch; pricing and general availability have not been disclosed.
What makes Ottava different from da Vinci?
Ottava's four arms are integrated into the operating table itself rather than mounted on a boom or carts, stowing beneath the table and reportedly saving 30-50% of OR space. Da Vinci counters with a far larger installed base and broader indications.
What procedures is Ottava cleared for?
Ten general surgery procedures, including Roux-en-Y gastric bypass, gastrectomy, gastric sleeve, cholecystectomy, splenectomy, small bowel resection, appendectomy, lysis of adhesions, fundoplication and hiatal hernia repair.
Did Ottava go through clinical trials?
Yes. A US IDE study begun in late 2024 supported the submission; in the 30-patient pivotal bariatric cohort, Ottava met its primary safety and performance endpoints with no conversions to non-robotic surgery. An inguinal hernia trial is ongoing.

Sources

  1. Johnson & Johnson — jnj.com, retrieved 2026-09-01
  2. Johnson & Johnson MedTech — jnjmedtech.com, retrieved 2026-09-01
  3. Johnson & Johnson — jnj.com, retrieved 2026-09-01
  4. MedTech Dive — medtechdive.com, retrieved 2026-09-01
  5. MassDevice — massdevice.com, retrieved 2026-09-01

Related medical robots

HYDROS Robotic System

PROCEPT BioRobotics · #1 in Medical

Robotic waterjet ablation (Aquablation therapy) of prostate tissue for benign prostatic hyperplasia (BPH)

Mako SmartRobotics

Stryker · #2 in Medical

Robotic-arm assisted orthopedic surgery: total knee, total hip, partial knee, spine and shoulder procedures

da Vinci 5

Intuitive Surgical · #3 in Medical

Robotic-assisted minimally invasive soft-tissue surgery across urology, gynecology, general surgery, thoracic and, since 2026, selected cardiac procedures

Hugo RAS

Medtronic · #4 in Medical

Robotic-assisted minimally invasive soft-tissue surgery; US indication currently covers urologic procedures such as prostatectomy, nephrectomy and cystectomy