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BioWorld - Wednesday, January 14, 2026
Home » Topics » Regulatory

Regulatory
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Da Vinci Xi robot - Intuitive Surgical

J&J’s Ottava robotic system approved for US pivotal trial

Nov. 13, 2024
By Annette Boyle
Johnson & Johnson received U.S. FDA investigational device exemption to begin the pivotal clinical trial for the Ottava robotic surgical system. If the trial goes well, Ottava could pose a significant challenge to decades-long dominance of the robotic surgical market by Intuitive Surgical Inc.’s Da Vinci system.
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3D illustration of transparent human torso with close up of spinal cord

Nevro wins CE mark for spinal cord stimulation technology

Nov. 13, 2024
By Shani Alexander
Nevro Corp. received CE mark certification for its HFX iQ spinal cord stimulation system that delivers pain relief.
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Cleerly Labs product suite

Cleerly scores win with four-MAC coverage of AI-QCT

Nov. 13, 2024
By Mark McCarty
Device makers are not necessarily fond of the need to acquire Medicare coverage by picking off one Medicare administrative contractor at a time, but Cleerly Labs Inc. worked this path with gusto.
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European Union flag with wooden gavel

New notified body survey highlights role of poor-quality submissions

Nov. 13, 2024
By Mark McCarty
The European Commission posted the results of the latest survey of notified bodies, and as the saying goes, there’s good news and bad news.
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Woman about to receive a vaccine
Immune

CSPC’s HPV mRNA vaccine candidate cleared to enter clinic in China

Nov. 13, 2024
CSPC Pharmaceutical Group Ltd.’s SYS-6026 has obtained clearance from China’s National Medical Products Administration (NMPA) to enter clinical trials for the treatment of high-grade squamous intraepithelial lesions associated with human papillomavirus (HPV) type 16 or 18.
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3D illustration showing presence of tumor inside prostate gland
Diagnostics

Antelope Surgical’s AS-1986NS cleared to enter clinic

Nov. 13, 2024
Antelope Surgical Solutions Inc. has received commercial IND approval from the FDA for its novel prostate cancer technology, AS-1986NS. AS1986NS, a fluorescent and lutetium-175 bearing drug, will be evaluated in trials with the aim of addressing prostate cancer identification and surgical margin delineation.
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FDA lifts clinical hold on Carsgen’s CAR Ts following warnings

Nov. 12, 2024
By Tamra Sami
The FDA has lifted a clinical hold on Carsgen Therapeutics Holdings Ltd.’s. CAR T products after issuing the company a warning letter following a December 2023 FDA inspection that found the company violated good manufacturing practices at its Research Triangle Park facility in Durham, N.C.
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Laptop displaying FDA logo

​Owens & Minor draws FDA warning for lack of sterilization documentation

Nov. 12, 2024
By Mark McCarty
The U.S. FDA’s Nov. 1 warning letter to Owens & Minor Inc. criticized the company for a lack of documentation that two components of convenience kits had been validated for sterilization with ethylene oxide.
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Momentis Surgical Anovo robotic platform

Momentis gains FDA clearance for second generation surgical robot

Nov. 12, 2024
By Shani Alexander
Momentis Surgical Ltd. received 510 (k) clearance from the U.S. FDA for the second-generation of the Anovo robotic surgical platform. The upgraded system allows surgeons to experience enhanced ergonomics with integrated haptic feedback, creating more intuitive control of the robotic arms during surgical procedures.
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AI biotech research concept with lightbulb and digital background

Tempus Labs wins reversal of patent rejection over machine learning

Nov. 12, 2024
By Mark McCarty
Abstract ideas are not generally eligible for patents in the U.S., but a recent dispute heard by the U.S. Patent Trial and Appeal Board adds a new twist to the question.
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