510(k) · Cleared
ClearedGrasping Forceps
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Micro-Tech (Nanjing) Co., Ltd. · OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered
Cleared on Jan 21, 2016 as substantially equivalent to K120084 (United States Endoscopy Group, Inc., 2012) after a 115-day review. Its family tree reaches back 1 generation to 2012. 1 later device descends from it.
- Decided
- Jan 21, 2016
- Review
- 115 days
- Class
- Class II
- Product code
- OCZ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K120084 (2012). 1 later device descends from it, 1 citing it directly.
- Root · 1 generation backK120084 Endoscopic Retrieval DeviceUnited States Endoscopy Group, Inc. · 2012
- This deviceK152802 Grasping ForcepsMicro-Tech (Nanjing) Co., Ltd. · 2016
- Descendant · cites it directly · 0 of its ownK191900 Single Use Grasping ForcepsZhejiang Chuangxiang Medical Technology Co., Ltd. · 2020
Most influential descendants
Showing 1 of 1 · See all- K191900Single Use Grasping ForcepsZhejiang Chuangxiang Medical Technology Co., Ltd. · 2020 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K120084 | Endoscopic Retrieval Device | United States Endoscopy Group, Inc. | 2012 | — |
| 0 (this device) | K152802 | Grasping Forceps | Micro-Tech (Nanjing) Co., Ltd. | 2016 | — |
| +1 | K191900 | Single Use Grasping Forceps | Zhejiang Chuangxiang Medical Technology Co., Ltd. | 2020 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2020 | 1 | 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 OCZ? 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 OCZ device
- #1 K252800 KARL STORZ Endoscopic Accessories for Urologyscore 11.5 · 1 generation · 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 |
|---|---|---|---|
| * | K120084 | Endoscopic Retrieval DeviceSummary page 5…vel (SAL) of 10-6 and placed in a sterility maintenance package to ensure a shelf life of 5 years. 6. Identification of Predicate Device 510(k) Number:K120084 Trade Name: The US Endoscopy Endoscopic Retrieval Device Regulation Name: Endoscope and accessories 7. Non-Clin… | 2012 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K191900 | Single Use Grasping Forceps | 2020 | 0 |
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?
How does its category compare?
All OCZ devicesOCZ Endoscopic Grasping/Cutting Instrument, Non-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.
FDA decisions per year · OCZ
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · OCZ
Too few OCZ 510(k)s in any year since 2007 to give a median.
Recalls per year · OCZ
17in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · OCZ
34in 2025
MAUDE reports naming product code OCZ, 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 | 0 | — | 0 | 1 |
| 2008 | 1 | — | 0 | 2 |
| 2009 | 0 | — | 0 | 2 |
| 2010 | 1 | — | 0 | 2 |
| 2011 | 1 | — | 0 | 0 |
| 2012 | 1 | — | 0 | 6 |
| 2013 | 0 | — | 0 | 4 |
| 2014 | 2 | — | 0 | 1 |
| 2015 | 1 | — | 0 | 242 |
| 2016 | 1 | — | 0 | 759 |
| 2017 | 0 | — | 0 | 734 |
| 2018 | 0 | — | 0 | 252 |
| 2019 | 0 | — | 0 | 15 |
| 2020 | 1 | — | 0 | 21 |
| 2021 | 0 | — | 0 | 20 |
| 2022 | 0 | — | 17 | 33 |
| 2023 | 0 | — | 0 | 25 |
| 2024 | 1 | — | 0 | 37 |
| 2025 | 0 | — | 0 | 34 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
Grasping Forceps device is intended to be used to grasp tissue, retrieve foreign bodies, and remove tissue from within the gastrointestinal tract.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K152802 · printed Nov 3, 2026
Cite this page
510(k) Report. “K152802: Grasping Forceps.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K152802
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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