Atlas FDA

COATED APEX PROBE

FDA 510(k) clearance K890735 · decided 1989-04-19

Clearance details

K-number
K890735
Device name
COATED APEX PROBE
Applicant
Analytic Technology
Decision
Substantially Equivalent
Date received
1989-02-13
Decision date
1989-04-19
Days to decision
65 days
Clearance type
Traditional
Product code
LQY
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Redmond, WA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Apex Locator (FindPex) (K252224)Changzhou Sifary Medical Technology Co., Ltd.2026-04-08
Apex Locator (K242383)Shenzhen Rogin Medical Co., Ltd.2025-03-07
Electronic Apex Locator (Alpha Apex I) (K242765)SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.2025-01-17
Apex Locator (K231990)Cefla S.C.2024-02-13
Apex Locator (AL-Pex), Apex Locator (AL-Pex+) (K232717)Changzhou Haili Medical Co., Ltd.2023-12-22
Root Apex Locator (K212178)Foshan Coxo Medical Instrument Co., Ltd.2022-07-20
EQ-PEX (K210789)Meta Systems Co., Ltd.2021-10-20
BOMEDENT Apex locator, WISMY Apex locator (K203836)Changzhou Bomedent Medical Technology Co.,Ltd2021-03-30
Propex IQ Apex Locator (K191806)Dentsply Sirona2019-10-03
Apex Locator, DPEX III (K181087)Guilin Woodpecker Medical Instrument Co., Ltd.2018-12-18
Dr’s Finder NEO (K171867)Good Doctors Co., Ltd.2018-03-30
Dr's Finder (K151274)Good Doctors Co., Ltd.2016-02-04

Recalls involving this device

No recalls on record reference this clearance.