510(k) Report

510(k) · Cleared

Cleared

Connected OR Hub with Device and Voice Control

K192172510(k) SpecialCleared Sep 9, 201928-day reviewClass II21 CFR 876.1500

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Stryker · GCJ Laparoscope, General & Plastic Surgery

Cleared on Sep 9, 2019 as substantially equivalent to K181258 (Stryker, 2018) after a 28-day review. Its family tree reaches back 10 generations to 1993. 9 later devices descend from it.

Decided
Sep 9, 2019
Review
28 days
Class
Class II
Product code
GCJ
Recalls
None
Predicates
1

Its longest line of descent runs back 10 generations to K931783 (1993). 13 ancestors in all. 9 later devices descend from it, 2 citing it directly.

  1. Root · 10 generations backK931783 Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc. · 1993
  2. 6 generations between
  3. 3 generations backK121893 Stryker SDC3 HD Information Management SystemStryker Endoscopy · 2012
  4. 2 generations backK160332 Stryker SDC3 HD Information Management System with Wireless Device…Stryker Endoscopy · 2016
  5. 1 generation backK181258 ConnectedOR Hub with Device and Voice ControlStryker · 2018
  6. This deviceK192172 Connected OR Hub with Device and Voice ControlStryker · 2019
  7. Descendant · cites it directly · 8 of its ownK201434 Connected OR Hub with Voice Control, Connected OR Hub with Device…Stryker · 2020
  8. Descendant · cites it directly · 6 of its ownK212055 Connected OR Hub with Device and Voice ControlStryker Corporation · 2021
  9. Descendant · 2 generations on · 5 of its ownK220108 SDC4K Information Management System with Device and Voice Control…Stryker Endoscopy · 2022
  10. Descendant · 2 generations on · 4 of its ownK222079 Connected OR Hub with Device and Voice Control, SDC4K Information…Stryker Endoscopy · 2022
  11. Descendant · 3 generations on · 3 of its ownK230886 Connected OR Hub with Device and Voice Control; SDC4K Information…Stryker Endoscopy · 2023
Show all 10 generations
  1. Root · 10 generations backK931783 Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc. · 1993
  2. 9 generations backK960655 Aesop System and AccessoriesComputer Motion, Inc. · 1996
  3. 8 generations backK973700 Hermes Operating Room Control CenterComputer Motion, Inc. · 1998
  4. 7 generations backK980787 Hermes Operating Room Control Center with the Wom 20L InsufflatorComputer Motion, Inc. · 1998
  5. 6 generations backK990691 Hermes Operating Room Control CenterComputer Motion, Inc. · 1999
  6. 5 generations backK991444 Hermes Control Center, with Control of the Aesop 3000HR (Hermes…Computer Motion, Inc. · 1999
  7. 4 generations backK022393 Merdoc SystemStryker Endoscopy · 2003
  8. 3 generations backK121893 Stryker SDC3 HD Information Management SystemStryker Endoscopy · 2012
  9. 2 generations backK160332 Stryker SDC3 HD Information Management System with Wireless Device…Stryker Endoscopy · 2016
  10. 1 generation backK181258 ConnectedOR Hub with Device and Voice ControlStryker · 2018
  11. This deviceK192172 Connected OR Hub with Device and Voice ControlStryker · 2019

Showing 5 of 9 descendants. See all descendants

Descendants cleared per year

2020: 12021: 12022: 22023: 22024: 12026: 2
2020high 2 (2022) · low 0 (2025)2026

Most influential descendants

Showing 5 of 9 · See all
  • K201434Connected OR Hub with Voice Control, Connected OR Hub with Device ControlStryker · 2020 · cites it directly8descendants
  • K212055Connected OR Hub with Device and Voice ControlStryker Corporation · 2021 · cites it directly6descendants
  • K220108SDC4K Information Management System with Device and Voice Control PackageStryker Endoscopy · 2022 · 2 generations on5descendants
  • K222079Connected OR Hub with Device and Voice Control, SDC4K Information Management System with…Stryker Endoscopy · 2022 · 2 generations on4descendants
  • K230886Connected OR Hub with Device and Voice Control; SDC4K Information Management System with…Stryker Endoscopy · 2023 · 3 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K931783Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc.1993—
−9K960655Aesop System and AccessoriesComputer Motion, Inc.1996—
−8K973700Hermes Operating Room Control CenterComputer Motion, Inc.1998—
−7K980787Hermes Operating Room Control Center with the Wom 20L InsufflatorComputer Motion, Inc.1998—
−6K990691Hermes Operating Room Control CenterComputer Motion, Inc.1999—
−5K991444Hermes Control Center, with Control of the Aesop 3000HR (Hermes Ready).Computer Motion, Inc.1999—
−4K022393Merdoc SystemStryker Endoscopy2003—
−3K121893Stryker SDC3 HD Information Management SystemStryker Endoscopy2012—
−2K160332Stryker SDC3 HD Information Management System with Wireless Device Control…Stryker Endoscopy2016—
−1K181258ConnectedOR Hub with Device and Voice ControlStryker2018—
0 (this device)K192172Connected OR Hub with Device and Voice ControlStryker2019—
+1K201434Connected OR Hub with Voice Control, Connected OR Hub with Device ControlStryker2020—
+1K212055Connected OR Hub with Device and Voice ControlStryker Corporation2021—
+2K220108SDC4K Information Management System with Device and Voice Control PackageStryker Endoscopy2022—
+2K222079Connected OR Hub with Device and Voice Control, SDC4K Information Management…Stryker Endoscopy2022—
+3K230886Connected OR Hub with Device and Voice Control; SDC4K Information Management…Stryker Endoscopy2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
199720

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202110
202220
202320
202410
202620
FIG. 1 — Lineage of K192172, 1993–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in GCJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new GCJ device

  1. #1 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 21 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K181258ConnectedOR Hub with Device and Voice Control
Summary page 4
…nt Product Code HRX Predicate Device: Name of Device Stryker Connected OR Hub with Device and Voice Control, K181258 Note: The predicate device has not been subject to a design-related recall. Device Description: The Connected OR Hub with Device…
Stryker2018—

Also cleared against K181258: 2 other devices →

What descends from it? (9)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K201434Connected OR Hub with Voice Control, Connected OR Hub with Device ControlStryker20208
K212055Connected OR Hub with Device and Voice ControlStryker Corporation20216

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 26 years and passes through 3 companies; a new generation was cleared every 2.4 years on median.
  • None of the 13 ancestors has a recall.
  • Of its descendants, K201434 (Stryker, 2020) has gone furthest, with 8 descendants of its own.
  • 2 other devices also cite its predicate K181258.

How does its category compare?

All GCJ devices

GCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · GCJ

21in 2025

2007: 182008: 192009: 212010: 242011: 152012: 172013: 152014: 192015: 262016: 272017: 202018: 212019: 152020: 282021: 182022: 202023: 312024: 292025: 212026 (partial year): 26
2007high 31 (2023) · low 15 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GCJ

108in 2025

2007: 42 days median2008: 73 days median2009: 85 days median2010: 122 days median2011: 113 days median2012: 88 days median2013: 93 days median2014: 90 days median2015: 76 days median2016: 99 days median2017: 77 days median2018: 88 days median2019: 60 days median2020: 61 days median2021: 116 days median2022: 103 days median2023: 109 days median2024: 90 days median2025: 108 days median2026 (partial year): 122 days median
2007high 122 (2010) · low 42 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GCJ

5in 2025

2007: 122008: 162009: 62010: 302011: 92012: 12013: 7, 1 Class I2014: 22016: 52017: 12018: 12022: 12023: 12025: 52026 (partial year): 1
2007high 30 (2010) · low 0 (2015)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · GCJ

5,860in 2025

2007: 1,6392008: 1,3192009: 1,9952010: 2,6572011: 2,1332012: 1,5262013: 1,5652014: 1,7142015: 1,7102016: 2,0802017: 3,4682018: 2,5622019: 2,5782020: 2,6182021: 3,4312022: 3,9452023: 6,0022024: 6,0472025: 5,860
2007high 6,047 (2024) · low 1,319 (2008)2025

MAUDE reports naming product code GCJ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071842121,639
20081973161,319
2009218561,995
201024122302,657
20111511392,133
2012178811,526
201315937 (1)1,565
2014199021,714
2015267601,710
2016279952,080
2017207713,468
2018218812,562
2019156002,578
2020286102,618
20211811603,431
20222010313,945
20233110916,002
2024299006,047
20252110855,860
2026261221—

What is it indicated for?

The use of the Connected OR Hub with Device and Voice Control system is to allow for voice control and remote control of medical device settings by surgeons or operating room personnel, thereby eliminating the need to manually operate those devices compatible with the Connected OR Hub with Device and Voice Control or to rely on verbal communication between the surgeon and other operating room personnel in order to adjust the surgical equipment. It also has additional digital documentation functionality to electronically capture, transfer, store and display medical device data (non-medical device function), which is independent of the functions or parameters of any attached Stryker device.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192172: Connected OR Hub with Device and Voice Control.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K192172

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026