510(k) Report

510(k) · Cleared

Cleared

Harrington Hook Clamp

K781448510(k) TraditionalCleared Sep 27, 197835-day reviewClass I21 CFR 878.4800

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

Orthopedic Equipment Co., Inc. · GEN Forceps, General & Plastic Surgery

Cleared on Sep 27, 1978 after a 35-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 4 later devices descend from it.

Decided
Sep 27, 1978
Review
35 days
Class
Class I
Product code
GEN
Recalls
None
Predicates
0

4 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2016: 1 descendant cleared2018: 1 descendant cleared2022: 1 descendant cleared2026: 1 descendant cleared19801990200020102020
  1. This deviceK781448 Harrington Hook ClampOrthopedic Equipment Co., Inc. · 1978
  2. Descendant · cites it directly · 3 of its ownK161028 K2M Growing Spine SystemK2m, Inc. · 2016
  3. Descendant · 2 generations on · 2 of its ownK181068 CREO® Stabilization System, REVERE® Stabilization SystemGlobus Medical, Inc. · 2018
  4. Descendant · 3 generations on · 0 of its ownK253739 SCRIPT™ Rods, CREO™ Stabilization System, REVERE® Stabilization…Globus Medical, Inc. · 2026
  5. Descendant · 3 generations on · 0 of its ownK213196 MARVEL™ Growing RodsGlobus Medical, Inc. · 2022

Most influential descendants

Showing 4 of 4 · See all
  • K161028K2M Growing Spine SystemK2m, Inc. · 2016 · cites it directly3descendants
  • K181068CREO® Stabilization System, REVERE® Stabilization SystemGlobus Medical, Inc. · 2018 · 2 generations on2descendants
  • K253739SCRIPT™ Rods, CREO™ Stabilization System, REVERE® Stabilization System, REVERE® 4.5…Globus Medical, Inc. · 2026 · 3 generations on0descendants
  • K213196MARVEL™ Growing RodsGlobus Medical, Inc. · 2022 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K781448Harrington Hook ClampOrthopedic Equipment Co., Inc.1978—
+1K161028K2M Growing Spine SystemK2m, Inc.2016—
+2K181068CREO® Stabilization System, REVERE® Stabilization SystemGlobus Medical, Inc.2018—
+3K253739SCRIPT™ Rods, CREO™ Stabilization System, REVERE® Stabilization System…Globus Medical, Inc.2026—
+3K213196MARVEL™ Growing RodsGlobus Medical, Inc.2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201810
202210
202610
FIG. 1 — Lineage of K781448, 1978–2026Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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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? (4)

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

NumberDeviceApplicantDecidedDescendants
K161028K2M Growing Spine SystemK2m, Inc.20163

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, K161028 (K2m, Inc., 2016) has gone furthest, with 3 descendants of its own.

How does its category compare?

All GEN devices

GEN Forceps, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GEN

FDA has decided no GEN device since 2007.

Median 510(k) review, days · GEN

Too few GEN 510(k)s in any year since 2007 to give a median.

Recalls per year · GEN

3in 2024

2010: 12016: 12018: 12024: 3
2007high 3 (2024) · low 0 (2007)2026

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

Adverse event reports per year · GEN

30in 2025

2007: 262008: 152009: 222010: 212011: 162012: 182013: 242014: 232015: 272016: 192017: 342018: 162019: 182020: 62021: 202022: 182023: 252024: 202025: 30
2007high 34 (2017) · low 6 (2020)2025

MAUDE reports naming product code GEN, 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—026
20080—015
20090—022
20100—121
20110—016
20120—018
20130—024
20140—023
20150—027
20160—119
20170—034
20180—116
20190—018
20200—06
20210—020
20220—018
20230—025
20240—320
20250—030
20260—0—

More from Orthopedic Equipment Co., Inc.

45 FDA decisions under this applicant name. See the company

  • K834035Universal Self-Aligning Acetabular ComOrthopedic Equipment Co., Inc. · 1984
  • K841189Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
  • K800530Schlein Tri-Surface AnkleOrthopedic Equipment Co., Inc. · 1980
  • K781445SpreaderOrthopedic Equipment Co., Inc. · 1979
  • K790247Tourniquet Test GageOrthopedic Equipment Co., Inc. · 1979

Recent decisions in GEN

The GEN category page

  • K031828Naturalase LP ND:Yag LaserFocus Medical, LLC · 2003
  • K953962ForcepsBiopsys Medical, Inc. · 1995
  • K932385Suture Removing ForcepsRocket of London, Ltd. · 1993
  • K904723ForcepsMinto Research & Development, Inc. · 1991
  • K911159Palpation ProbeNorthgate Technologies, Inc. · 1991

https://510kreport.com/device/K781448 · printed Nov 6, 2026

Cite this page

510(k) Report. “K781448: Harrington Hook Clamp.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K781448

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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