510(k) · Cleared
ClearedEndohub- 1.0 Endoscopic Video Camera System with Video Capture
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Pointe Conception Medical, Inc. · GCJ Laparoscope, General & Plastic Surgery
Cleared on Aug 15, 2007 as substantially equivalent to K031098 (Linvatec Corp., 2003) after a 48-day review. Its family tree reaches back 3 generations to 1995. 15 later devices descend from it.
- Decided
- Aug 15, 2007
- Review
- 48 days
- Class
- Class II
- Product code
- GCJ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K950862 (1995). 4 ancestors in all. 15 later devices descend from it, 1 citing it directly.
- Root · 3 generations backK950862 Karl Storz Endovision Tricam, Model 20221101 (20221001, Pal Format)…Karl Storz Imaging, Inc. · 1995
- 2 generations backK983566 3-Chip Video CameraStryker Endoscopy · 1999 · Recalled
- 1 generation backK031098 3-CCD Digital Camera SystemLinvatec Corp. · 2003
- This deviceK071756 Endohub- 1.0 Endoscopic Video Camera System with Video CapturePointe Conception Medical, Inc. · 2007
- Descendant · cites it directly · 14 of its ownK153218 Arthrex Synergy UHD4 SystemArthrex, Inc. · 2016
- Descendant · 2 generations on · 12 of its ownK190645 Arthrex NanoScope SystemArthrex, Inc. · 2019
- Descendant · 3 generations on · 11 of its ownK201134 Arthrex NanoScope SystemArthrex, Inc. · 2020
- Descendant · 2 generations on · 5 of its ownK202582 Arthrex SynergyID Endoscopic Imaging SystemArthrex, Inc. · 2021
- Descendant · 4 generations on · 4 of its ownK243008 Arthrex NanoScope SystemArthrex, Inc. · 2025
Showing 5 of 15 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 15 · See all- K153218Arthrex Synergy UHD4 SystemArthrex, Inc. · 2016 · cites it directly14descendants
- K190645Arthrex NanoScope SystemArthrex, Inc. · 2019 · 2 generations on12descendants
- K201134Arthrex NanoScope SystemArthrex, Inc. · 2020 · 3 generations on11descendants
- K202582Arthrex SynergyID Endoscopic Imaging SystemArthrex, Inc. · 2021 · 2 generations on5descendants
- K243008Arthrex NanoScope SystemArthrex, Inc. · 2025 · 4 generations on4descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K950862 | Karl Storz Endovision Tricam, Model 20221101 (20221001, Pal Format) Color… | Karl Storz Imaging, Inc. | 1995 | — |
| −2 | K983566 | 3-Chip Video Camera | Stryker Endoscopy | 1999 | 1 |
| −1 | K031098 | 3-CCD Digital Camera System | Linvatec Corp. | 2003 | — |
| 0 (this device) | K071756 | Endohub- 1.0 Endoscopic Video Camera System with Video Capture | Pointe Conception Medical, Inc. | 2007 | — |
| +1 | K153218 | Arthrex Synergy UHD4 System | Arthrex, Inc. | 2016 | — |
| +2 | K190645 | Arthrex NanoScope System | Arthrex, Inc. | 2019 | — |
| +3 | K201134 | Arthrex NanoScope System | Arthrex, Inc. | 2020 | — |
| +2 | K202582 | Arthrex SynergyID Endoscopic Imaging System | Arthrex, Inc. | 2021 | — |
| +4 | K243008 | Arthrex NanoScope System | Arthrex, Inc. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 1 | 0 |
| 2019 | 1 | 0 |
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2023 | 1 | 0 |
| 2024 | 2 | 0 |
| 2025 | 6 | 0 |
| 2026 | 2 | 0 |
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 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 21 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K031098 | 3-CCD Digital Camera SystemSummary page 2…Manufa er Substantial Equivalence comments K031098 Autoclavable 3-CCD Digital Camera Linvatec System… | 2003 |
What descends from it? (15)
See all 151 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K153218 | Arthrex Synergy UHD4 System | 2016 | 14 |
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 12 years and passes through 4 companies; a new generation was cleared every 4.2 years on median.
- 1 of the 4 ancestors has a recall of any class.
- Of its descendants, K153218 (Arthrex, Inc., 2016) has gone furthest, with 14 descendants of its own.
- 1 other device also cites its predicate K031098.
How does its category compare?
All GCJ devicesGCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · GCJ
21in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GCJ
108in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GCJ
5in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · GCJ
5,860in 2025
MAUDE reports naming product code GCJ, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 18 | 42 | 12 | 1,639 |
| 2008 | 19 | 73 | 16 | 1,319 |
| 2009 | 21 | 85 | 6 | 1,995 |
| 2010 | 24 | 122 | 30 | 2,657 |
| 2011 | 15 | 113 | 9 | 2,133 |
| 2012 | 17 | 88 | 1 | 1,526 |
| 2013 | 15 | 93 | 7 (1) | 1,565 |
| 2014 | 19 | 90 | 2 | 1,714 |
| 2015 | 26 | 76 | 0 | 1,710 |
| 2016 | 27 | 99 | 5 | 2,080 |
| 2017 | 20 | 77 | 1 | 3,468 |
| 2018 | 21 | 88 | 1 | 2,562 |
| 2019 | 15 | 60 | 0 | 2,578 |
| 2020 | 28 | 61 | 0 | 2,618 |
| 2021 | 18 | 116 | 0 | 3,431 |
| 2022 | 20 | 103 | 1 | 3,945 |
| 2023 | 31 | 109 | 1 | 6,002 |
| 2024 | 29 | 90 | 0 | 6,047 |
| 2025 | 21 | 108 | 5 | 5,860 |
| 2026 | 26 | 122 | 1 | — |
What is it indicated for?
The Endohub-1.0 Endoscopic Video Camera with Video Capture is intended to be used as an endoscopic video camera in a variety of endoscopic surgical procedures, including but not limited to; orthopedic, laparoscopic, urologic, sinuscopic and plastic surgery. The device is also intended to be used as an accessory for microscopic
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K071756 · printed Nov 5, 2026
Cite this page
510(k) Report. “K071756: Endohub- 1.0 Endoscopic Video Camera System with Video Capture.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K071756
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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