Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list U.S. Mfg. & Management, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 2, 1992: CONTROLLED PASSIVE MOTION MACHINE.
| Apr 2, 1992 | CONTROLLED PASSIVE MOTION MACHINEK920860 · BXB | 510(k) clearances |
| Jan 5, 1988 | FLUID SAMPLING PACKK874436 · KSS | 510(k) clearances |
| Jul 24, 1986 | MODIFIED I.V. START, RE-START, PEDI AND GERI-KITK862335 · | 510(k) clearances |
| Aug 30, 1985 | I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KIK853242 · | 510(k) clearances |
| Sep 24, 1984 | VENI-SHIELDK842999 · KMK | 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
