Atlas FDA

SECURIPIN

FDA 510(k) clearance K844457 · decided 1984-12-27

Clearance details

K-number
K844457
Device name
SECURIPIN
Applicant
Hughes Int'L, Inc.
Decision
Substantially Equivalent
Date received
1984-11-16
Decision date
1984-12-27
Days to decision
41 days
Clearance type
Traditional
Product code
EBL
Device class
1
Regulation number
872.3740
Medical specialty
Dental
Advisory committee
Dental
Location
Hunt Valley, MD, 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
CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS) (K002693)Cbs Intl. B.V.2000-11-09
DENTAURUM JACKET CROWN & ROOT POSTS (K952868)Dentauraum, Inc.1995-07-19
ROOT CANAL POST (K924376)The Thera Group1993-11-22
PROSTHETIC RESTORATION DEVICE (K895283)Swiss Precision Mfg. Corp.1990-02-14
PLASTIC TOOTH REINFORCEMENT KIT (K895758)Nanzee Dental Products1989-12-20
ELGILOY (K883074)Dale T. Dupuis1988-08-09
VIVADENT FILPIN (K863831)Vivadent (Usa), Inc.1986-10-14
MARKLEY THREADED WIRE (K830773)Almore Intl., Inc.1983-04-28
REINFORCING PIN (K822412)Filhol1982-08-30
SAFE-T-PINS RETENTIVE PIN SYSTEM (K760723)Parkell, Inc.1976-10-21

Recalls involving this device

No recalls on record reference this clearance.