Atlas FDA

ORTHO WAX

FDA 510(k) clearance K924024 · decided 1992-11-17

Clearance details

K-number
K924024
Device name
ORTHO WAX
Applicant
Heraeus Kulzer, Inc.
Decision
Substantially Equivalent
Date received
1992-08-11
Decision date
1992-11-17
Days to decision
98 days
Clearance type
Traditional
Product code
EGD
Device class
1
Regulation number
872.6890
Medical specialty
Dental
Advisory committee
Dental
Location
South Bend, IN, 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
BRACE EZE (K020009)Udent, Inc.2002-02-11
GLENROE ORTHO-SIL (K945535)Glenroe Technologies1995-01-27
BURNOUT MATERIAL (K923586)Dentsply Intl.1992-09-29
SALIVA-STIM (K914892)Orion Diagnostica, Inc.1992-09-02
BITE RIM WAX (K922380)Dentsply Intl.1992-06-16
PALAVIT G (K914513)Heraeus Kulzer, Inc.1992-03-19
INTRAORAL DENTAL WAX (K910676)Pemaco, Inc.1991-08-21
PALAVIT GLC (K904928)Kulzer, Inc.1991-06-06
PEMACO 2000 INTRAORAL DENTAL WAX (K895562)Pemaco, Inc.1989-11-06
PEMACO 3000 INTRAORAL DENTAL WAX (K895561)Pemaco, Inc.1989-11-06
PEMACO BITE WAX SHEETS (K895563)Pemaco, Inc.1989-11-06
PEMACO ECONOMY BASE PLATE WAX-MEDIUM SOFT (K895566)Pemaco, Inc.1989-11-06

Recalls involving this device

No recalls on record reference this clearance.