Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Physician Engineered Products, Inc. with 8 510(k) clearances and 1 device recall. The most recent is a device recall dated Aug 31, 2013: Bright Embrace, a Single Bili Light for newborn phototherapy Distributed by: Physici….
| Aug 31, 2013 | Bright Embrace, a Single Bili Light for newborn phototherapy Distributed by: Physician Engineered Products, Inc., Model SBL60Class II · Upper limit for ambient temperature for use of the device was printed incorrectly in the instructions | Device recalls |
| Feb 3, 2012 | BRIGHT EMBRACE MODEL SBL60K110550 · LBI | 510(k) clearances |
| Apr 23, 2010 | BILI-MIRROR MODEL BLM-1K093618 · LBI | 510(k) clearances |
| May 20, 1998 | ULTRA BILI LIGHTK974830 · LBI | 510(k) clearances |
| Nov 21, 1988 | MODIFIED REFLUX REDUCERK883818 · FMS | 510(k) clearances |
| Jun 20, 1988 | RETROFIT BABY FACE SHIELD (RFS)K882291 · LBI | 510(k) clearances |
| Jun 16, 1988 | RESUSCITATION BAG CONTROLLER (RBC)K882278 · BTM | 510(k) clearances |
| Dec 11, 1987 | INSTITUTIONAL BILI LIGHT (IBL)K873700 · LBI | 510(k) clearances |
| Jun 17, 1985 | HOME BILI LIGHTS-MODEL 100K850599 · LBI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
