Surgical Theater, Inc.
Surgical Theater, Inc. holds FDA 510(k) medical device clearances, first cleared 2020, most recent 2025, with 7 FDA device recalls on record.
Top product codes for Surgical Theater, Inc.
FDA recalls by Surgical Theater, Inc.
- Z-0321-2026 — Surgical Navigation Advanced Platform Patient Engagement (PE SNAP), software version SNP.3.12.0, imaging processing radiological system
- Z-0323-2026 — Endo Surgical Navigation Advanced Platform Patient Engagement (EndoSNAP), software version SNP.1.12.0, imaging processing radiological system
- Z-0319-2026 — SuRgical Planner (SRP), software version SRP.7.12.0, imaging processing radiological system
- Z-0325-2026 — Surgical Planner, BrainSTORM, software version BST.9.3.0, orthopedic augmented reality
- Z-0320-2026 — Surgical Navigation Advanced Platform (SNAP), software version SNP.3.12.0, imaging processing radiological system
- Z-0322-2026 — SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR SNAP), software version SNP.1.12.0, imaging processing radiological system
- Z-0324-2026 — SpineAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR SNAP), software version SPR.1.2.0, orthopedic augmented reality
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Surgical Theater, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.