Techfit Digital Surgery, Inc.

FDA Regulatory Profile

Techfit Digital Surgery, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 27, 2025.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250297TECHFIT Patient-Specific Cranial SystemOctober 27, 2025
K242263TECHFIT DISRP® SystemDecember 11, 2024
K230276TECHFIT DISRP® SystemJune 23, 2023
K222577TECHFIT Diagnostic ModelsJanuary 6, 2023
K220199AFFINITY Proximal Tibia SystemMarch 21, 2022