Atlas FDA

BIOFORCE WIRE

FDA 510(k) clearance K920905 · decided 1992-11-04

Clearance details

K-number
K920905
Device name
BIOFORCE WIRE
Applicant
Gac Intl., Inc.
Decision
Substantially Equivalent
Date received
1992-02-27
Decision date
1992-11-04
Days to decision
251 days
Clearance type
Traditional
Product code
DZC
Device class
1
Regulation number
872.5410
Medical specialty
Dental
Advisory committee
Dental
Location
Central Islip, NY, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Gac Intl.

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
HYPERELASTIC WIRE (K112640)Ormco Corp.2011-11-16
HAWLEY RETAINER ORTHODONTIC APPLICANCE KIT (K943334)Jay H. Geller1994-10-05
NITINOL, NITI (K935638)Highland Metals1994-05-18
DENTAURUM STEEL LIGATURE WIRES (K935140)Dentauraum, Inc.1994-02-04
DENTAURUM WIRES (K935142)Dentauraum, Inc.1994-01-31
FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIRE (K934265)Flexmedics1994-01-21
NITI COIL SPRINGS (K933374)Highland Metals1993-11-19
STAINLESS STEEL ARCHES REPACKER RELABETER (K933377)Highland Metals1993-11-16
REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER (K933378)Highland Metals1993-11-12
REVERSE SURVE NITI ARCH WIRE (K933380)Highland Metals1993-11-12
STAINLESS STEEL ARCHES (K933379)Highland Metals1993-11-12
NITI ARCH WIRE ON A SPOOL (K933376)Highland Metals1993-11-12

Recalls involving this device

No recalls on record reference this clearance.