# K142204: Bioceptive Suction Cervical Retractor

- Pathway: 510(k) (Traditional)
- Applicant: Bioceptive, Inc.
- Decided: Dec 19, 2014 after 130 days
- Product code: HDC (Tenaculum, Uterine)
- Device class: 2
- Regulation: 21 CFR 884.4530
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Bioceptive Suction Cervical Retractor is indicated to snare, grasp, hold and manipulate cervical tissue.

Source page: https://510kreport.com/device/K142204
Methodology: https://510kreport.com/methodology