510(k) Report

510(k) · Cleared

Cleared

Curette, Proposed Tis-U-Trap, Metal

K760264510(k) TraditionalCleared Oct 6, 197677-day reviewClass II21 CFR 884.1175

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

Milex Products, Inc. · HHK Curette, Suction, Endometrial (And Accessories)

Cleared on Oct 6, 1976 after a 77-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Oct 6, 1976
Review
77 days
Class
Class II
Product code
HHK
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1998: 1 descendant cleared19801990200020102020
  1. This deviceK760264 Curette, Proposed Tis-U-Trap, MetalMilex Products, Inc. · 1976
  2. Descendant · cites it directly · 0 of its ownK980096 Oac (Optical Aspirating Curette)Imagyn Medical Technologies, Inc. · 1998

Most influential descendants

Showing 1 of 1 · See all
  • K980096Oac (Optical Aspirating Curette)Imagyn Medical Technologies, Inc. · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K760264Curette, Proposed Tis-U-Trap, MetalMilex Products, Inc.1976—
+1K980096Oac (Optical Aspirating Curette)Imagyn Medical Technologies, Inc.1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
FIG. 1 — Lineage of K760264, 1976–1998Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 HHK? 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 HHK device

  1. #1 K251882 Uterine Aspiration Setscore 10.5 · 2 generations · 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? (1)

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

NumberDeviceApplicantDecidedDescendants
K980096Oac (Optical Aspirating Curette)Imagyn Medical Technologies, Inc.19980

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, K980096 (Imagyn Medical Technologies, Inc., 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All HHK devices

HHK Curette, Suction, Endometrial (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HHK

1in 2025

2010: 12011: 12020: 22024: 12025: 1
2007high 2 (2020) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HHK

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

Recalls per year · HHK

1in 2022

2014: 22022: 1
2007high 2 (2014) · low 0 (2007)2026

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

Adverse event reports per year · HHK

9in 2025

2008: 22013: 12015: 22016: 12017: 22018: 12019: 42021: 12022: 22023: 12024: 42025: 9
2007high 9 (2025) · low 0 (2007)2025

MAUDE reports naming product code HHK, 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—00
20080—02
20090—00
20101—00
20111—00
20120—00
20130—01
20140—20
20150—02
20160—01
20170—02
20180—01
20190—04
20202—00
20210—01
20220—12
20230—01
20241—04
20251—09
20260—0—
Cite this page

510(k) Report. “K760264: Curette, Proposed Tis-U-Trap, Metal.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K760264

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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