HENRIETTA, N.Y.– Turbett Surgical has received 510(k) clearance from the U.S. Food and Drug Administration for its enhanced Instrument Pod portfolio, including the TS1500, TS1200, and TS1000 models. The regulatory green light supports newly validated performance claims that significantly upgrade the system’s capabilities in surgical instrument management.
Among the key updates, the TS1200 now has a certified weight capacity of up to 300 pounds, more than doubling its previous limit of 120 pounds. The increased load capability allows for more efficient handling of larger and heavier surgical instrument sets.
Additionally, the enhanced system includes expanded lumen validation, covering a broader range of rigid and flexible lumens, specifically those measuring 0.7 mm x 500 mm and 1.0 mm x 850 mm. This expanded support offers increased versatility for healthcare facilities managing delicate scopes and specialty instruments.
Turbett Surgical said the clearance reflects its commitment to performance, safety, and innovation in operating room efficiency. The company’s Instrument Pod systems are designed to reduce reliance on disposable surgical blue wrap, streamline workflow, and lower environmental impact.
The improvements benefit a wide range of healthcare professionals. Hospital administrators can achieve cost savings and waste reduction, while surgical teams gain more reliable access to instruments, reducing workflow interruptions. Sterile processing department professionals also benefit from reduced physical strain and simplified processes.
Turbett’s enhanced systems are currently in use at military hospitals, regional medical centers, and ambulatory surgery centers, reflecting a growing shift toward more sustainable and efficient surgical instrument strategies. (IANS)
