Atlas FDA

SET CANAL SEALER PASTE

FDA 510(k) clearance K862129 · decided 1986-07-22

Clearance details

K-number
K862129
Device name
SET CANAL SEALER PASTE
Applicant
Endo Technic Corp.
Decision
Substantially Equivalent
Date received
1986-06-04
Decision date
1986-07-22
Days to decision
48 days
Clearance type
Traditional
Product code
EKM
Device class
1
Regulation number
872.3850
Medical specialty
Dental
Advisory committee
Dental
Location
Natick, MA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Endo Technic Corp.

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
EI DOWNPAK BARRIER SLEEVES (K073369)Hu-Friedy Mfg. Co., Inc.2008-02-27
DOWN PAK (K070246)Endo Twinn B.V.2007-02-16
TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE) (K051573)Dr. Howard Martin, P.A.2006-06-26
ENDO TWINN (K042870)Endo Twinn B.V.2005-01-11
FIBERFILL SGP (K023819)Pentron Clinical Technologies2003-03-26
ANTIBACTERIAL GUTTA PERCHA (K971641)Dr. Howard Martin, P.A.1997-07-21
THERMAPREP PLUS OVEN (K970134)Tulsa Dental Products, Ltd.1997-03-21
INJECT-R FILL (K931742)Union Broach, Div. Moyco Industries, Inc.1993-05-27
MICRODOSE RC-EZ (K924825)Unicep1993-03-05
TOUCH 'N HEAT MODEL 5002, MODIFICATION (K915243)Analytic Technology1992-01-21
THERMAPREP (K910224)Tulsa Dental Products, Ltd.1991-03-29
THERMAFIL ENDODONTIC OBTURATOR (K900986)Tulsa Dental Products, Ltd.1990-11-13

Recalls involving this device

No recalls on record reference this clearance.