510(k) Report

510(k) · Cleared

Cleared

Connected OR Hub with Device and Voice Control, SDC4K Information Management System with Device and Voice Control

K232157510(k) SpecialCleared Aug 18, 202329-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 Corporation · GCJ Laparoscope, General & Plastic Surgery

Cleared on Aug 18, 2023 as substantially equivalent to K230886 (Stryker Endoscopy, 2023) after a 29-day review. Its family tree reaches back 16 generations to 1993. 2 later devices descend from it.

Decided
Aug 18, 2023
Review
29 days
Class
Class II
Product code
GCJ
Recalls
None
Predicates
1

Its longest line of descent runs back 16 generations to K931783 (1993). 22 ancestors in all, the oldest K864584 (1986). 2 later devices descend from it, 1 citing it directly.

Other ancestors, by generationDescendants, by generation 5 generations back: 1 other ancestor6 generations back: 1 other ancestor7 generations back: 1 other ancestor9 generations back: 1 other ancestor10 generations back: 1 other ancestor12 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant K230886 · Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control · Stryker Endoscopy · 2023K222079 · Connected OR Hub with Device and Voice Control, SDC4K Information Management System with Device and Voice Control · Stryker Endoscopy · 2022K220108 · SDC4K Information Management System with Device and Voice Control Package · Stryker Endoscopy · 2022K212055 · Connected OR Hub with Device and Voice Control · Stryker Corporation · 2021K201434 · Connected OR Hub with Voice Control, Connected OR Hub with Device Control · Stryker · 2020K192172 · Connected OR Hub with Device and Voice Control · Stryker · 2019K181258 · ConnectedOR Hub with Device and Voice Control · Stryker · 2018K160332 · Stryker SDC3 HD Information Management System with Wireless Device Control Capability · Stryker Endoscopy · 2016K121893 · Stryker SDC3 HD Information Management System · Stryker Endoscopy · 2012K022393 · Merdoc System · Stryker Endoscopy · 2003K991444 · Hermes Control Center, with Control of the Aesop 3000HR (Hermes Ready). · Computer Motion, Inc. · 1999K990691 · Hermes Operating Room Control Center · Computer Motion, Inc. · 1999K980787 · Hermes Operating Room Control Center with the Wom 20L Insufflator · Computer Motion, Inc. · 1998K973700 · Hermes Operating Room Control Center · Computer Motion, Inc. · 1998K960655 · Aesop System and Accessories · Computer Motion, Inc. · 1996K931783 · Aesop (Automated Endoscopic System for Optimal Pos · Computer Motion, Inc. · 1993−15−10−50
  1. Root · 16 generations backK931783 Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc. · 1993
  2. 12 generations between
  3. 3 generations backK220108 SDC4K Information Management System with Device and Voice Control…Stryker Endoscopy · 2022
  4. 2 generations backK222079 Connected OR Hub with Device and Voice Control, SDC4K Information…Stryker Endoscopy · 2022
  5. 1 generation backK230886 Connected OR Hub with Device and Voice Control; SDC4K Information…Stryker Endoscopy · 2023
  6. This deviceK232157 Connected OR Hub with Device and Voice Control, SDC4K Information…Stryker Corporation · 2023
  7. Descendant · cites it directly · 1 of its ownK241401 Connected OR Hub with Device and Voice Control; SDC4K Information…Stryker Endoscopy · 2024
  8. Descendant · 2 generations on · 0 of its ownK254014 Connected OR Hub with Device and Voice Control; SDC4K Information…Stryker Endoscopy · 2026
Show all 16 generations
  1. Root · 16 generations backK931783 Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc. · 1993
  2. 15 generations backK960655 Aesop System and AccessoriesComputer Motion, Inc. · 1996
  3. 14 generations backK973700 Hermes Operating Room Control CenterComputer Motion, Inc. · 1998
  4. 13 generations backK980787 Hermes Operating Room Control Center with the Wom 20L InsufflatorComputer Motion, Inc. · 1998
  5. 12 generations backK990691 Hermes Operating Room Control CenterComputer Motion, Inc. · 1999
  6. 11 generations backK991444 Hermes Control Center, with Control of the Aesop 3000HR (Hermes…Computer Motion, Inc. · 1999
  7. 10 generations backK022393 Merdoc SystemStryker Endoscopy · 2003
  8. 9 generations backK121893 Stryker SDC3 HD Information Management SystemStryker Endoscopy · 2012
  9. 8 generations backK160332 Stryker SDC3 HD Information Management System with Wireless Device…Stryker Endoscopy · 2016
  10. 7 generations backK181258 ConnectedOR Hub with Device and Voice ControlStryker · 2018
  11. 6 generations backK192172 Connected OR Hub with Device and Voice ControlStryker · 2019
  12. 5 generations backK201434 Connected OR Hub with Voice Control, Connected OR Hub with Device…Stryker · 2020
  13. 4 generations backK212055 Connected OR Hub with Device and Voice ControlStryker Corporation · 2021
  14. 3 generations backK220108 SDC4K Information Management System with Device and Voice Control…Stryker Endoscopy · 2022
  15. 2 generations backK222079 Connected OR Hub with Device and Voice Control, SDC4K Information…Stryker Endoscopy · 2022
  16. 1 generation backK230886 Connected OR Hub with Device and Voice Control; SDC4K Information…Stryker Endoscopy · 2023
  17. This deviceK232157 Connected OR Hub with Device and Voice Control, SDC4K Information…Stryker Corporation · 2023

Most influential descendants

Showing 2 of 2 · See all
  • K241401Connected OR Hub with Device and Voice Control; SDC4K Information Management System with…Stryker Endoscopy · 2024 · cites it directly1descendant
  • K254014Connected OR Hub with Device and Voice Control; SDC4K Information Management System with…Stryker Endoscopy · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−16K931783Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc.1993—
−15K960655Aesop System and AccessoriesComputer Motion, Inc.1996—
−14K973700Hermes Operating Room Control CenterComputer Motion, Inc.1998—
−13K980787Hermes Operating Room Control Center with the Wom 20L InsufflatorComputer Motion, Inc.1998—
−12K990691Hermes Operating Room Control CenterComputer Motion, Inc.1999—
−11K991444Hermes Control Center, with Control of the Aesop 3000HR (Hermes Ready).Computer Motion, Inc.1999—
−10K022393Merdoc SystemStryker Endoscopy2003—
−9K121893Stryker SDC3 HD Information Management SystemStryker Endoscopy2012—
−8K160332Stryker SDC3 HD Information Management System with Wireless Device Control…Stryker Endoscopy2016—
−7K181258ConnectedOR Hub with Device and Voice ControlStryker2018—
−6K192172Connected OR Hub with Device and Voice ControlStryker2019—
−5K201434Connected OR Hub with Voice Control, Connected OR Hub with Device ControlStryker2020—
−4K212055Connected OR Hub with Device and Voice ControlStryker Corporation2021—
−3K220108SDC4K Information Management System with Device and Voice Control PackageStryker Endoscopy2022—
−2K222079Connected OR Hub with Device and Voice Control, SDC4K Information Management…Stryker Endoscopy2022—
−1K230886Connected OR Hub with Device and Voice Control; SDC4K Information Management…Stryker Endoscopy2023—
0 (this device)K232157Connected OR Hub with Device and Voice Control, SDC4K Information Management…Stryker Corporation2023—
+1K241401Connected OR Hub with Device and Voice Control; SDC4K Information Management…Stryker Endoscopy2024—
+2K254014Connected OR Hub with Device and Voice Control; SDC4K Information Management…Stryker Endoscopy2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
199620
199720
201310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
202610
FIG. 1 — Lineage of K232157, 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
*K230886Connected OR Hub with Device and Voice Control; SDC4K Information Management System with…
Summary page 4
…ber 876.1500 Product Code GCJ I Legally Marketed Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K230886 Connected OR Hub with Device and Voice Control; SDC4K InfoE GCJ Device Description Summary 21 CFR 807.92(a)(4) The Connected OR…
Stryker Endoscopy2023—

Also cleared against K230886: 1 other device →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K241401Connected OR Hub with Device and Voice Control; SDC4K Information Management System with…Stryker Endoscopy20241

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 30 years and passes through 4 companies; a new generation was cleared every 11 months on median.
  • None of the 22 ancestors has a recall.
  • Of its descendants, K241401 (Stryker Endoscopy, 2024) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K230886.

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. 2023, 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 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…

Read the full statement (212 words)

The use of the Connected OR Hub with Device and Voice Control 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.

The use of the SDC4K Information Management System with Device and Voice Control 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 SDC4K Information Management System 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 read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K232157: Connected OR Hub with Device and Voice Control, SDC4K Information Management System 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/K232157

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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