Atlas FDA

da Vinci Force Feedback Instruments

FDA 510(k) clearance K253986 · decided 2026-03-11

Clearance details

K-number
K253986
Device name
da Vinci Force Feedback Instruments
Applicant
Intuitive Surgical, Inc.
Decision
Substantially Equivalent
Date received
2025-12-12
Decision date
2026-03-11
Days to decision
89 days
Clearance type
Traditional
Product code
NAY
Device class
2
Regulation number
876.1500
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Sunnyvale, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
da Vinci Surgical System, Model IS5000 (K261824)Intuitive Surgical, Inc.2026-07-31
da Vinci Firefly Imaging System (K260695)Intuitive Surgical2026-05-22
Senhance Ultrasonic System (K254192)Asensus Surgical2026-05-12
da Vinci Surgical System (IS5000) (K251739)Intuitive Surgical, Inc.2026-01-16
da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator (K253556)Intuitive Surgical, Inc.2026-01-16
da Vinci SP Surgical System (SP1098) (K252675)Intuitive Surgical, Inc.2025-12-15
da Vinci SP Surgical System (SP1098) (K252069)Intuitive Surgical, Inc.2025-12-02
da Vinci SP Surgical System (SP1098) (K251426)Intuitive Surgical, Inc.2025-10-03
da Vinci SP Surgical System (SP1098) (K251817)Intuitive Surgical, Inc.2025-09-10
da Vinci Surgical System (IS5000) (K251227)Intuitive Surgical, Inc.2025-09-08
da Vinci SP Surgical System (SP1098) (K251324)Intuitive Surgical, Inc.2025-08-29
da Vinci SP Firefly Imaging System (K252350)Intuitive Surgical, Inc.2025-08-28

Recalls involving this device

No recalls on record reference this clearance.