510(k) Report

510(k) · Cleared

Cleared

Olympus FG Series of Rat Tooth Grasping Forceps

K955051510(k) TraditionalCleared Jan 18, 199673-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

Olympus America, Inc. · OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered

Cleared on Jan 18, 1996 after a 73-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 11 later devices descend from it.

Decided
Jan 18, 1996
Review
73 days
Class
Class II
Product code
OCZ
Recalls
None
Predicates
0

11 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 1996: 2 descendants cleared2006: 2 descendants cleared2008: 1 descendant cleared2010: 4 descendants cleared2009: 1 descendant cleared2011: 1 descendant cleared1995200020052010201520202025
  1. This deviceK955051 Olympus FG Series of Rat Tooth Grasping ForcepsOlympus America, Inc. · 1996
  2. Descendant · cites it directly · 9 of its ownK962474 Olympus FG Series of Rat Tooth Grasping Forceps (Urology)Olympus America, Inc. · 1996
  3. Descendant · 2 generations on · 5 of its ownK061276 G-Prox Endoscopic GrasperUsgi Medical · 2006
  4. Descendant · 2 generations on · 2 of its ownK061268 G-Lix Tissue GrasperUsgi Medical · 2006
  5. Descendant · 3 generations on · 1 of its ownK100251 G-Cath Tissue Anchor Delivery Catheter, Models 205302, 205333Usgi Medical · 2010
  6. Descendant · 3 generations on · 1 of its ownK093018 G-Prox Endoscopic Grasper, Model 205333Usgi Medical · 2009

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

1996: 22006: 22008: 12009: 12010: 42011: 1
1996high 4 (2010) · low 0 (1997)2026

Most influential descendants

Showing 5 of 11 · See all
  • K962474Olympus FG Series of Rat Tooth Grasping Forceps (Urology)Olympus America, Inc. · 1996 · cites it directly9descendants
  • K061276G-Prox Endoscopic GrasperUsgi Medical · 2006 · 2 generations on5descendants
  • K061268G-Lix Tissue GrasperUsgi Medical · 2006 · 2 generations on2descendants
  • K100251G-Cath Tissue Anchor Delivery Catheter, Models 205302, 205333Usgi Medical · 2010 · 3 generations on1descendant
  • K093018G-Prox Endoscopic Grasper, Model 205333Usgi Medical · 2009 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K955051Olympus FG Series of Rat Tooth Grasping ForcepsOlympus America, Inc.1996—
+1K962474Olympus FG Series of Rat Tooth Grasping Forceps (Urology)Olympus America, Inc.1996—
+2K061276G-Prox Endoscopic GrasperUsgi Medical2006—
+2K061268G-Lix Tissue GrasperUsgi Medical2006—
+3K100251G-Cath Tissue Anchor Delivery Catheter, Models 205302, 205333Usgi Medical2010—
+3K093018G-Prox Endoscopic Grasper, Model 205333Usgi Medical2009—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199620
200620
200810
200910
201040
201110
FIG. 1 — Lineage of K955051, 1996–2011Source: 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), 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. #1 K252800 KARL STORZ Endoscopic Accessories for Urologyscore 11.4 · 1 generation · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (11)

See all 11

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

NumberDeviceApplicantDecidedDescendants
K962474Olympus FG Series of Rat Tooth Grasping Forceps (Urology)Olympus America, Inc.19969
K962485Olympus FG Series of Rat Tooth Grasping Forceps (Ent)Olympus America, Inc.19960

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?

  • Of its descendants, K962474 (Olympus America, Inc., 1996) has gone furthest, with 9 descendants of its own.

How does its category compare?

All OCZ devices

OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · OCZ

1in 2024

2008: 12010: 12011: 12012: 12014: 22015: 12016: 12020: 12024: 12026 (partial year): 1
2007high 2 (2014) · low 0 (2007)2026

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

2022: 17
2007high 17 (2022) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · OCZ

34in 2025

2007: 12008: 22009: 22010: 22012: 62013: 42014: 12015: 2422016: 7592017: 7342018: 2522019: 152020: 212021: 202022: 332023: 252024: 372025: 34
2007high 759 (2016) · low 0 (2011)2025

MAUDE reports naming product code OCZ, 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
20070—01
20081—02
20090—02
20101—02
20111—00
20121—06
20130—04
20142—01
20151—0242
20161—0759
20170—0734
20180—0252
20190—015
20201—021
20210—020
20220—1733
20230—025
20241—037
20250—034
20261—0—
Cite this page

510(k) Report. “K955051: Olympus FG Series of Rat Tooth Grasping Forceps.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K955051

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026