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FDA 510(k)

CoolSeal Trinity

K-Number: K231012 · 2023-11-15

ApplicantBolder Surgical, LLC
Decision Date2023-11-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CoolSeal Trinity is a medical device manufactured by Bolder Surgical, LLC. It received FDA 510(k) clearance on 2023-11-15 under approval number K231012. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CoolSeal Trinity?

CoolSeal Trinity is a medical device that received FDA 510(k) clearance on 2023-11-15. It is manufactured by Bolder Surgical, LLC. The 510(k) number is K231012.

When was CoolSeal Trinity approved by the FDA?

CoolSeal Trinity received FDA 510(k) clearance on 2023-11-15, under approval number K231012.

What company makes CoolSeal Trinity?

CoolSeal Trinity is manufactured by Bolder Surgical, LLC.

What is the FDA product code for CoolSeal Trinity?

The FDA product code for CoolSeal Trinity is GEI.

Other Devices by Bolder Surgical, LLC

K202114CoolSeal Generator/CSL-200-50, CoolSeal Trinity (30 cm shaft)/CSL-TR105-30, CoolSeal Trinity (37 cm shaft)/CSL-TR105-37, CoolSeal Trinity (44 cm shaft)/CSL-TR105-44, CoolSeal Mini (20cm shaft)/CSL-MN103-20 K211579CoolSeal Trinity (30 cm shaft), CoolSeal Trinity (37 cm shaft), CoolSeal Trinity (44 cm shaft) K203183CoolSeal Trinity (30 cm shaft, 37 cm shaft, and 44 cm shaft) K203640CoolSeal Reveal

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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