Atlas FDA

QuickSleeper 5

FDA 510(k) clearance K243427 · decided 2025-08-01

Clearance details

K-number
K243427
Device name
QuickSleeper 5
Applicant
Dentalhitec
Decision
Substantially Equivalent
Date received
2024-11-05
Decision date
2025-08-01
Days to decision
269 days
Clearance type
Traditional
Product code
EGM
Device class
2
Regulation number
872.4475
Medical specialty
Dental
Advisory committee
Dental
Location
Mazieres En Mauges, FR
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
W&H HANDPIECE ANESTO, MODEL: RA-5 (K083811)W&H Dentalwerk Buermoos GmbH2010-01-14
CYBERJET LOCAL ANESTHESIA SYSTEM (K964802)Intra Vantage, Inc.1997-05-27
HYPODERMIC JET INJECTION APPARATUS (K962017)American Jet Injector Corp.1996-07-26
PAROJECT ANESTHETIC SYRINGE (K904279)Ronvig Instruments, Ltd.1990-12-07
HENKE-JECT PRESSURE SYRINGE (MODIFICATION) (K864294)Smith & Nephew, Inc.1987-11-04
GRADTECH SYRINGE SYSTEM (K864732)Gradtech1987-04-15
INSTRUMENTATIONS UNLIMITED SYRINGE SYSTEM (K864861)Instrumentations Unltd.1987-02-13
JSB JET SYRINGE (K834361)C.B.S. Biotechnics, Inc.1984-03-05
MAYO SCISSOR STRAIGHT 6 3/4 (K821273)Conphar, Inc.1982-05-28
MIZZY SYRIJET MARK IV (K790193)Mizzy, Inc.1979-04-23

Recalls involving this device

No recalls on record reference this clearance.